ClinVar for Gene (Select 100652770) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273862	NM_001943.5(DSG2):c.2989G>C (p.Gly997Arg)	DSG2, DSG2-AS1 (G997R)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3273861	NM_001943.5(DSG2):c.2380G>A (p.Asp794Asn)	DSG2, DSG2-AS1 (D794N)	Single nucleotide variant (non-coding transcript variant +1 more)	Cardiovascular phenotype	GUncertain significance
Select item 3273859	NM_001943.5(DSG2):c.2983C>T (p.His995Tyr)	DSG2, DSG2-AS1 (H995Y)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3273857	NM_001943.5(DSG2):c.3235G>C (p.Ala1079Pro)	DSG2, DSG2-AS1 (A1079P)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3273855	NM_001943.5(DSG2):c.2916T>C (p.Ser972=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3273853	NM_001943.5(DSG2):c.2425G>A (p.Ala809Thr)	DSG2, DSG2-AS1 (A809T)	Single nucleotide variant (non-coding transcript variant +1 more)	Cardiovascular phenotype	GUncertain significance
Select item 3236598	NM_001943.5(DSG2):c.3016C>T (p.Gln1006Ter)	DSG2, DSG2-AS1 (Q1006*)	Single nucleotide variant (nonsense)	Arrhythmogenic right ventricular dysplasia 10	GLikely pathogenic
Select item 3234096	NM_001943.5(DSG2):c.2300_2304del (p.Leu767fs)	DSG2, DSG2-AS1 (L767fs)	Deletion (frameshift variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely pathogenic
Select item 3221944	NM_001943.5(DSG2):c.3271G>A (p.Glu1091Lys)	DSG2, DSG2-AS1 (E1091K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3221943	NM_001943.5(DSG2):c.3174A>C (p.Gln1058His)	DSG2, DSG2-AS1 (Q1058H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3221942	NM_001943.5(DSG2):c.2322T>C (p.Asn774=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype	GLikely benign
Select item 3221940	NM_001943.5(DSG2):c.2105C>G (p.Ala702Gly)	DSG2, DSG2-AS1 (A702G)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 3221939	NM_001943.5(DSG2):c.2036G>T (p.Gly679Val)	DSG2, DSG2-AS1 (G679V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GLikely benign
Select item 3075287	NM_001943.5(DSG2):c.3065T>C (p.Phe1022Ser)	DSG2, DSG2-AS1 (F1022S)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3075213	NM_001943.5(DSG2):c.2477T>C (p.Leu826Ser)	DSG2, DSG2-AS1 (L826S)	Single nucleotide variant (non-coding transcript variant +1 more)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3075178	NM_001943.5(DSG2):c.3138G>A (p.Val1046=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3075167	NM_001943.5(DSG2):c.2799G>A (p.Val933=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3074984	NM_001943.5(DSG2):c.2505A>T (p.Thr835=)	DSG2, DSG2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3074926	NM_001943.5(DSG2):c.2839C>T (p.Pro947Ser)	DSG2, DSG2-AS1 (P947S)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3074893	NM_001943.5(DSG2):c.2996C>G (p.Ser999Trp)	DSG2, DSG2-AS1 (S999W)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3074866	NM_001943.5(DSG2):c.2573C>T (p.Ala858Val)	DSG2, DSG2-AS1 (A858V)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3074660	NM_001943.5(DSG2):c.2119G>A (p.Gly707Arg)	DSG2, DSG2-AS1 (G707R)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3074644	NM_001943.5(DSG2):c.2666C>A (p.Pro889Gln)	DSG2-AS1, DSG2 (P889Q)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3074507	NM_001943.5(DSG2):c.2101T>A (p.Ser701Thr)	DSG2, DSG2-AS1 (S701T)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3074361	NM_001943.5(DSG2):c.3006G>T (p.Leu1002=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3074023	NM_001943.5(DSG2):c.3151_3152dup (p.Leu1051_Ala1052insTer)	DSG2, DSG2-AS1	Duplication (frameshift variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3073846	NM_001943.5(DSG2):c.2981C>T (p.Pro994Leu)	DSG2, DSG2-AS1 (P994L)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3073750	NM_001943.5(DSG2):c.2851G>C (p.Val951Leu)	DSG2, DSG2-AS1 (V951L)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3073710	NM_001943.5(DSG2):c.2239A>C (p.Thr747Pro)	DSG2, DSG2-AS1 (T747P)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3073425	NM_001943.5(DSG2):c.2248G>A (p.Ala750Thr)	DSG2, DSG2-AS1 (A750T)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3073364	NM_001943.5(DSG2):c.2751G>C (p.Ala917=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3073103	NM_001943.5(DSG2):c.2193G>C (p.Gln731His)	DSG2, DSG2-AS1 (Q731H)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3073017	NM_001943.5(DSG2):c.3303C>T (p.Thr1101=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3072912	NM_001943.5(DSG2):c.2367T>G (p.Asn789Lys)	DSG2, DSG2-AS1 (N789K)	Single nucleotide variant (non-coding transcript variant +1 more)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3072680	NM_001943.5(DSG2):c.3315C>G (p.Thr1105=)	DSG2-AS1, DSG2	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3072301	NM_001943.5(DSG2):c.3109A>G (p.Asn1037Asp)	DSG2, DSG2-AS1 (N1037D)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3072029	NM_001943.5(DSG2):c.2471G>T (p.Arg824Leu)	DSG2, DSG2-AS1 (R824L)	Single nucleotide variant (non-coding transcript variant +1 more)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3071969	NM_001943.5(DSG2):c.3308del (p.Ser1103fs)	DSG2, DSG2-AS1 (S1103fs)	Deletion (frameshift variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3071849	NM_001943.5(DSG2):c.2169C>G (p.Ser723Arg)	DSG2, DSG2-AS1 (S723R)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3071532	NM_001943.5(DSG2):c.2750C>A (p.Ala917Glu)	DSG2-AS1, DSG2 (A917E)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3071208	NM_001943.5(DSG2):c.2135C>T (p.Ser712Phe)	DSG2, DSG2-AS1 (S712F)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3070900	NM_001943.5(DSG2):c.2009C>T (p.Pro670Leu)	DSG2, DSG2-AS1 (P670L)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3070858	NM_001943.5(DSG2):c.3338T>C (p.Val1113Ala)	DSG2, DSG2-AS1 (V1113A)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3070819	NM_001943.5(DSG2):c.2288C>T (p.Ala763Val)	DSG2, DSG2-AS1 (A763V)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3070750	NM_001943.5(DSG2):c.2859G>A (p.Leu953=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3070711	NM_001943.5(DSG2):c.2081C>A (p.Ala694Asp)	DSG2, DSG2-AS1 (A694D)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3070560	NM_001943.5(DSG2):c.2520C>T (p.Cys840=)	DSG2, DSG2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3070113	NM_001943.5(DSG2):c.3169C>G (p.Leu1057Val)	DSG2, DSG2-AS1 (L1057V)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3070084	NM_001943.5(DSG2):c.2693A>G (p.Asn898Ser)	DSG2, DSG2-AS1 (N898S)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3069975	NM_001943.5(DSG2):c.2058A>C (p.Gly686=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular cardiomyopathy	GLikely benign
Select item 3069894	NM_001943.5(DSG2):c.2156A>G (p.Glu719Gly)	DSG2-AS1, DSG2 (E719G)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3069764	NM_001943.5(DSG2):c.3342_3344dup (p.Gln1114_His1115insGln)	DSG2, DSG2-AS1	Duplication (inframe_insertion)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3069759	NM_001943.5(DSG2):c.2554G>A (p.Glu852Lys)	DSG2, DSG2-AS1 (E852K)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3069682	NM_001943.5(DSG2):c.2002G>A (p.Val668Met)	DSG2-AS1, DSG2 (V668M)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3069550	NM_001943.5(DSG2):c.2444G>C (p.Ser815Thr)	DSG2, DSG2-AS1 (S815T)	Single nucleotide variant (non-coding transcript variant +1 more)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3069286	NM_001943.5(DSG2):c.2984A>C (p.His995Pro)	DSG2, DSG2-AS1 (H995P)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy	GUncertain significance
Select item 3030916	NM_001943.5(DSG2):c.*9C>T	DSG2, DSG2-AS1	Single nucleotide variant (3 prime UTR variant)	DSG2-related disorder	GLikely benign
Select item 3021486	NM_001943.5(DSG2):c.3330T>C (p.His1110=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 3019727	NM_001943.5(DSG2):c.3066C>T (p.Phe1022=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 3018664	NM_001943.5(DSG2):c.3227T>C (p.Val1076Ala)	DSG2, DSG2-AS1 (V1076A)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 3017463	NM_001943.5(DSG2):c.2737T>C (p.Ser913Pro)	DSG2, DSG2-AS1 (S913P)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 3015131	NM_001943.5(DSG2):c.3151C>A (p.Leu1051Ile)	DSG2, DSG2-AS1 (L1051I)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 3012637	NM_001943.5(DSG2):c.3350A>T (p.Tyr1117Phe)	DSG2, DSG2-AS1 (Y1117F)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 3003063	NM_001943.5(DSG2):c.2799G>T (p.Val933=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10 +1 more	GLikely benign
Select item 2996680	NM_001943.5(DSG2):c.3077G>A (p.Ser1026Asn)	DSG2, DSG2-AS1 (S1026N)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2971261	NM_001943.5(DSG2):c.3136G>A (p.Val1046Met)	DSG2, DSG2-AS1 (V1046M)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2969322	NM_001943.5(DSG2):c.2334+10_2334+11del	DSG2, DSG2-AS1	Deletion (intron variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 2966445	NM_001943.5(DSG2):c.2669T>G (p.Val890Gly)	DSG2, DSG2-AS1 (V890G)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2914344	NM_001943.5(DSG2):c.3160G>C (p.Ala1054Pro)	DSG2, DSG2-AS1 (A1054P)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular cardiomyopathy +1 more	GUncertain significance
Select item 2914071	NM_001943.5(DSG2):c.2492T>C (p.Leu831Pro)	DSG2, DSG2-AS1 (L831P)	Single nucleotide variant (non-coding transcript variant +1 more)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2908461	NM_001943.5(DSG2):c.2353G>A (p.Glu785Lys)	DSG2, DSG2-AS1 (E785K)	Single nucleotide variant (non-coding transcript variant +1 more)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2908162	NM_001943.5(DSG2):c.2979G>A (p.Gln993=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 2906632	NM_001943.5(DSG2):c.2075A>C (p.Lys692Thr)	DSG2, DSG2-AS1 (K692T)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2906250	NM_001943.5(DSG2):c.2730A>G (p.Arg910=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 2898651	NM_001943.5(DSG2):c.2222C>T (p.Thr741Ile)	DSG2, DSG2-AS1 (T741I)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2891861	NM_001943.5(DSG2):c.2334+2dup	DSG2, DSG2-AS1	Duplication (splice donor variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2883272	NM_001943.5(DSG2):c.2181T>C (p.Gly727=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 2877690	NM_001943.5(DSG2):c.2965G>C (p.Glu989Gln)	DSG2, DSG2-AS1 (E989Q)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2865546	NM_001943.5(DSG2):c.2908C>G (p.Pro970Ala)	DSG2, DSG2-AS1 (P970A)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2856332	NM_001943.5(DSG2):c.3060G>T (p.Glu1020Asp)	DSG2, DSG2-AS1 (E1020D)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2853752	NM_001943.5(DSG2):c.2009CAT[3] (p.Ser671_Phe672insSer)	DSG2, DSG2-AS1	Microsatellite (inframe_insertion)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2845513	NM_001943.5(DSG2):c.3018G>C (p.Gln1006His)	DSG2, DSG2-AS1 (Q1006H)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2828671	NM_001943.5(DSG2):c.3123dup (p.Gln1042fs)	DSG2, DSG2-AS1 (Q1042fs)	Duplication (frameshift variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2820874	NM_001943.5(DSG2):c.2343C>G (p.Ala781=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 2817943	NM_001943.5(DSG2):c.2124A>G (p.Gln708=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 2814815	NM_001943.5(DSG2):c.3013A>C (p.Thr1005Pro)	DSG2, DSG2-AS1 (T1005P)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2800073	NM_001943.5(DSG2):c.3222C>T (p.Thr1074=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 2784179	NM_001943.5(DSG2):c.2731T>C (p.Ser911Pro)	DSG2, DSG2-AS1 (S911P)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2780418	NM_001943.5(DSG2):c.3213dup (p.Arg1072Ter)	DSG2, DSG2-AS1 (R1072*)	Duplication (nonsense)	Arrhythmogenic right ventricular dysplasia 10	GUncertain significance
Select item 2775695	NM_001943.5(DSG2):c.3294T>C (p.Ser1098=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Arrhythmogenic right ventricular dysplasia 10	GLikely benign
Select item 2775250	NM_001943.5(DSG2):c.*2C>G	DSG2-AS1, DSG2	Single nucleotide variant (3 prime UTR variant)	Cardiomyopathy	GUncertain significance
Select item 2775249	NM_001943.5(DSG2):c.3305C>A (p.Thr1102Lys)	DSG2, DSG2-AS1 (T1102K)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 2775248	NM_001943.5(DSG2):c.3186G>T (p.Gln1062His)	DSG2-AS1, DSG2 (Q1062H)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 2775247	NM_001943.5(DSG2):c.3078C>G (p.Ser1026Arg)	DSG2, DSG2-AS1 (S1026R)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 2775246	NM_001943.5(DSG2):c.2971G>T (p.Val991Leu)	DSG2, DSG2-AS1 (V991L)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 2775245	NM_001943.5(DSG2):c.2914T>C (p.Ser972Pro)	DSG2-AS1, DSG2 (S972P)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 10 +1 more	GUncertain significance
Select item 2775244	NM_001943.5(DSG2):c.2877G>C (p.Gln959His)	DSG2-AS1, DSG2 (Q959H)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance
Select item 2775243	NM_001943.5(DSG2):c.2847C>T (p.Thr949=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GLikely benign
Select item 2775242	NM_001943.5(DSG2):c.2823C>T (p.Val941=)	DSG2, DSG2-AS1	Single nucleotide variant (synonymous variant)	Cardiomyopathy +1 more	GLikely benign
Select item 2775241	NM_001943.5(DSG2):c.2737T>A (p.Ser913Thr)	DSG2-AS1, DSG2 (S913T)	Single nucleotide variant (missense variant)	Cardiomyopathy	GUncertain significance

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