ClinVar Miner

List of variants reported as likely pathogenic for Left ventricular noncompaction cardiomyopathy

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Total variants: 6
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HGVS dbSNP
NM_000257.4(MYH7):c.1573G>A (p.Glu525Lys) rs606231324
NM_000257.4(MYH7):c.860A>G (p.Tyr287Cys) rs587782961
NM_000335.4(SCN5A):c.2174_2175TG[3] (p.Ile727fs) rs869025523
NM_001035.3(RYR2):c.14565T>G (p.Ile4855Met) rs730880199
NM_001267550.2(TTN):c.58259G>A (p.Trp19420Ter) rs869025544
NM_001267550.2(TTN):c.66975_66978del (p.Lys22326fs) rs587782986

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