ClinVar Miner

List of variants in gene HCN4, LOC105370890 studied for Brugada syndrome

Included ClinVar conditions (45):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.1191T>C (p.Tyr397=) rs142643511 0.00004
NM_005477.3(HCN4):c.1186C>A (p.Arg396=) rs750479244 0.00001
NM_005477.3(HCN4):c.1178G>A (p.Arg393His) rs786205804
NM_005477.3(HCN4):c.1188A>G (p.Arg396=)
NM_005477.3(HCN4):c.1190A>C (p.Tyr397Ser) rs2043016094
NM_005477.3(HCN4):c.1209+15C>A
NM_005477.3(HCN4):c.1209+17A>G
NM_005477.3(HCN4):c.1209+19C>A
NM_005477.3(HCN4):c.1209+20C>T
NM_005477.3(HCN4):c.1209+2_1209+3insGTGA rs786205418
NM_005477.3(HCN4):c.1209+3A>G
NM_005477.3(HCN4):c.1209+4A>G rs2043015976
NM_005477.3(HCN4):c.1209+7G>C

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