ClinVar Miner

List of variants reported as likely pathogenic for Cardiomyopathy, left ventricular noncompaction

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Total variants: 10
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NM_000116.5(TAFAZZIN):c.355G>A (p.Val119Met) rs1603377936
NM_000256.3(MYBPC3):c.1805C>T (p.Thr602Ile) rs730880551
NM_000257.4(MYH7):c.1283C>A (p.Ala428Asp) rs727503266
NM_000257.4(MYH7):c.1573G>A (p.Glu525Lys) rs606231324
NM_000257.4(MYH7):c.860A>G (p.Tyr287Cys) rs587782961
NM_000335.5(SCN5A):c.2176_2177dup (p.Ile727fs) rs869025523
NM_001018005.2(TPM1):c.257C>T (p.Ala86Val) rs757577112
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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