C2750467[trait identifier] AND "Victorian Clinical Genetics Services, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 239179	NM_002471.4(MYH6):c.5476_5477delinsAA (p.Gly1826Asn)	MYH6 (G1826N)	Indel (missense variant)	Cardiomyopathy +5 more	GConflicting classifications of pathogenicity
Select item 191711	NM_002471.4(MYH6):c.4429C>T (p.Arg1477Cys)	MYH6 (R1477C)	Single nucleotide variant (missense variant)	Atrial septal defect 3 +6 more	GUncertain significance
Select item 164221	NM_002471.4(MYH6):c.4328C>A (p.Ala1443Asp)	MYH6 (A1443D)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +9 more	GUncertain significance
Select item 179607	NM_002471.4(MYH6):c.4082G>A (p.Arg1361His)	MYH6 (R1361H)	Single nucleotide variant (missense variant)	Atrial septal defect 3 +7 more	GUncertain significance
Select item 228889	NM_002471.4(MYH6):c.2086C>T (p.Arg696Cys)	MYH6 (R696C)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 14 +3 more	GUncertain significance
Select item 191720	NM_002471.4(MYH6):c.1328G>A (p.Arg443His)	MYH6 (R443H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1805286	NM_002471.4(MYH6):c.343T>C (p.Tyr115His)	LOC114827851, MYH6 (Y115H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 14	GUncertain significance
Select item 44474	NM_002471.4(MYH6):c.292G>A (p.Glu98Lys)	LOC114827851, MYH6 (E98K)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +8 more	GConflicting classifications of pathogenicity

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