ClinVar Miner

List of variants in gene combination ACTC1, LOC101928174 reported as likely benign for Familial restrictive cardiomyopathy

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Total variants: 14
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NM_005159.4(ACTC1):c.*1039G>A rs589759
NM_005159.4(ACTC1):c.*1445C>G rs8037241
NM_005159.4(ACTC1):c.*1674C>T rs112660730
NM_005159.4(ACTC1):c.*1682A>G rs533021
NM_005159.4(ACTC1):c.*2090A>G rs604689
NM_005159.4(ACTC1):c.*269C>T rs74009720
NM_005159.4(ACTC1):c.*388G>A rs1370154
NM_005159.4(ACTC1):c.*472T>C rs1370155
NM_005159.4(ACTC1):c.*868T>G rs80139141
NM_005159.4(ACTC1):c.*875G>C rs73387693
NM_005159.4(ACTC1):c.*918delA rs34323254
NM_005159.5(ACTC1):c.-57T>C rs113178069
NM_005159.5(ACTC1):c.809-58TG[21] rs59431308
NM_005159.5(ACTC1):c.927T>C (p.Pro309=) rs2307493

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