ClinVar Miner

List of variants reported as likely benign for dilated cardiomyopathy 1P

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001042475.3(CEP85L):c.1020+17189C>T rs9489434 0.01645
NM_001042475.3(CEP85L):c.1020+6360T>C rs28763979 0.01430
NM_001042475.3(CEP85L):c.1020+17280C>A rs551982604 0.00070
NM_002667.5(PLN):c.27C>T (p.Arg9=) rs145623013 0.00051
NM_002667.5(PLN):c.144C>T (p.Ile48=) rs141114252 0.00004
NM_002667.5(PLN):c.126C>T (p.Leu42=)
NM_002667.5(PLN):c.138T>C (p.Cys46=) rs1583047929
NM_002667.5(PLN):c.156C>A (p.Leu52=) rs1779077253
NM_002667.5(PLN):c.21C>T (p.Leu7=)
NM_002667.5(PLN):c.27C>A (p.Arg9=) rs145623013
NM_002667.5(PLN):c.33T>C (p.Ala11=)
NM_002667.5(PLN):c.45C>A (p.Ala15=)
NM_002667.5(PLN):c.51C>A (p.Thr17=)
NM_002667.5(PLN):c.69A>G (p.Gln23=)
NM_002667.5(PLN):c.90T>C (p.Asn30=) rs868301643

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