ClinVar Miner

List of variants reported as uncertain significance for congenital anomaly of cardiovascular system by Institute Of Molecular Biology And Genetics, Federal Almazov National Medical Research Centre

Included ClinVar conditions (333):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000116.5(TAFAZZIN):c.680dup (p.Tyr227Ter) rs1557194203

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