"PreventionGenetics, part of Exact Sciences"[submitter] AND "ADGRL2"[g - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058339	NM_001366006.2(ADGRL2):c.-9G>A	ADGRL2	Single nucleotide variant (5 prime UTR variant +1 more)	ADGRL2-related disorder	GLikely benign
Select item 3039606	NM_001366006.2(ADGRL2):c.321T>A (p.Thr107=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder	GLikely benign
Select item 2638900	NM_001366006.2(ADGRL2):c.1026C>T (p.Asn342=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder +1 more	GLikely benign
Select item 3055525	NM_001366006.2(ADGRL2):c.1320A>T (p.Gly440=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder	GBenign
Select item 3038465	NM_001366006.2(ADGRL2):c.1617C>T (p.Ser539=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder	GLikely benign
Select item 779220	NM_001366006.2(ADGRL2):c.1664A>G (p.Lys555Arg)	ADGRL2 (K551R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3045309	NM_001366006.2(ADGRL2):c.1734T>C (p.Asp578=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder	GBenign
Select item 3035183	NM_001366006.2(ADGRL2):c.1741C>T (p.Leu581=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder	GLikely benign
Select item 3051598	NM_001366006.2(ADGRL2):c.1890A>G (p.Lys630=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder	GLikely benign
Select item 2231793	NM_001366006.2(ADGRL2):c.2032G>T (p.Val678Leu)	ADGRL2 (V661L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3053105	NM_001366006.2(ADGRL2):c.2240G>T (p.Arg747Leu)	ADGRL2 (R730L +2 more)	Single nucleotide variant (missense variant +1 more)	ADGRL2-related disorder	GLikely benign
Select item 2638902	NM_001366006.2(ADGRL2):c.2298C>T (p.Ser766=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder +1 more	GBenign/Likely benign
Select item 3033758	NM_001366006.2(ADGRL2):c.2734-4G>A	ADGRL2	Single nucleotide variant (intron variant)	ADGRL2-related disorder	GLikely benign
Select item 3056444	NM_001366006.2(ADGRL2):c.3381A>G (p.Arg1127=)	ADGRL2	Single nucleotide variant (synonymous variant +1 more)	ADGRL2-related disorder	GBenign
Select item 3053882	NM_001366006.2(ADGRL2):c.3509-9_3509-8del	ADGRL2	Deletion (intron variant)	ADGRL2-related disorder	GLikely benign
Select item 3038680	NM_001366006.2(ADGRL2):c.3605A>G (p.Asn1202Ser)	ADGRL2 (N1202S +1 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GBenign
Select item 3056110	NM_001366006.2(ADGRL2):c.3637+309A>G	ADGRL2	Single nucleotide variant (synonymous variant +3 more)	ADGRL2-related disorder	GBenign
Select item 3042802	NM_001366006.2(ADGRL2):c.3641C>A (p.Thr1214Asn)	ADGRL2 (T1214N)	Single nucleotide variant (missense variant +1 more)	ADGRL2-related disorder	GLikely benign
Select item 3042178	NM_001366006.2(ADGRL2):c.3688G>C (p.Ala1230Pro)	ADGRL2 (A1164P +3 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GBenign
Select item 3048503	NM_001366006.2(ADGRL2):c.3726C>T (p.Asn1242=)	ADGRL2	Single nucleotide variant (synonymous variant +2 more)	ADGRL2-related disorder	GLikely benign
Select item 3043992	NM_001366006.2(ADGRL2):c.3746G>T (p.Gly1249Val)	ADGRL2 (G1183V +3 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GBenign
Select item 784951	NM_001366006.2(ADGRL2):c.3882G>A (p.Thr1294=)	ADGRL2	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 3052915	NM_001366006.2(ADGRL2):c.3889G>A (p.Val1297Ile)	ADGRL2 (V1231I +3 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GBenign
Select item 3045124	NM_001366006.2(ADGRL2):c.3913A>G (p.Ser1305Gly)	ADGRL2 (S1239G +3 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GBenign
Select item 3049645	NM_001366006.2(ADGRL2):c.4013T>C (p.Ile1338Thr)	ADGRL2 (I1272T +3 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GLikely benign
Select item 3037885	NM_001366006.2(ADGRL2):c.4082A>G (p.Tyr1361Cys)	ADGRL2 (Y1295C +3 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GBenign
Select item 3049584	NM_001366006.2(ADGRL2):c.4107T>C (p.Ala1369=)	ADGRL2	Single nucleotide variant (synonymous variant +2 more)	ADGRL2-related disorder	GLikely benign
Select item 3037276	NM_001366006.2(ADGRL2):c.4166G>A (p.Arg1389Lys)	ADGRL2 (R1323K +3 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GBenign
Select item 3043712	NM_001366006.2(ADGRL2):c.4180C>G (p.Pro1394Ala)	ADGRL2 (P1328A +3 more)	Single nucleotide variant (missense variant +2 more)	ADGRL2-related disorder	GBenign

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Items: 29