"Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU Münc - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 807634	NM_000257.4(MYH7):c.2642T>G (p.Leu881Arg)	LOC126861898, MYH7 (L881R)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1S	GLikely pathogenic
Select item 161326	NM_000257.4(MYH7):c.2608C>T (p.Arg870Cys)	LOC126861898, MYH7 (R870C)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy	GLikely pathogenic FDA Recognized database