rs397516088 - ClinVar

Format

Sort by

Choose Destination

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1488649	NM_000257.4(MYH7):c.1063G>C (p.Ala355Pro)	MYH7 (A355P)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 641658	NM_000257.4(MYH7):c.1063G>T (p.Ala355Ser)	MYH7 (A355S)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy	GUncertain significance
Select item 42820	NM_000257.4(MYH7):c.1063G>A (p.Ala355Thr)	MYH7 (A355T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GPathogenic/Likely pathogenic

Format

Sort by

Choose Destination

ClinVar