ClinVar Miner

List of variants reported as pathogenic for cardiomyopathy by Genetics and Genomics Program, Sidra Medicine

Included ClinVar conditions (522):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_032588.4(TRIM63):c.390C>G (p.Ile130Met) rs377334933 0.00003
NM_000256.3(MYBPC3):c.2526C>G (p.Tyr842Ter) rs373792537
NM_000256.3(MYBPC3):c.2905C>T (p.Gln969Ter) rs397515992
NM_001267550.2(TTN):c.72856G>T (p.Gly24286Ter) rs1198682781

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