ClinVar Miner

List of variants reported as not provided for Familial hypertrophic cardiomyopathy 10

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Total variants: 5
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HGVS dbSNP
NM_000432.3(MYL2):c.173G>A (p.Arg58Gln) rs104894369
NM_000432.3(MYL2):c.283C>G (p.Pro95Ala) rs121913658
NM_000432.3(MYL2):c.37G>A (p.Ala13Thr) rs104894363
NM_000432.3(MYL2):c.52T>C (p.Phe18Leu) rs104894370
NM_000432.3(MYL2):c.64G>A (p.Glu22Lys) rs104894368

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