ClinVar Miner

List of variants reported as likely pathogenic for Familial hypertrophic cardiomyopathy 10

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Total variants: 6
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HGVS dbSNP
NM_000432.3(MYL2):c.125G>A (p.Gly42Asp) rs863225117
NM_000432.3(MYL2):c.173G>T (p.Arg58Leu) rs104894369
NM_000432.3(MYL2):c.401A>C (p.Glu134Ala) rs143139258
NM_000432.3(MYL2):c.403-1G>C rs199474813
NM_000432.3(MYL2):c.488A>C (p.Glu163Ala) rs397516407
NM_000432.3(MYL2):c.64G>A (p.Glu22Lys) rs104894368

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