ClinVar Miner

List of variants in gene SCN3B reported as uncertain significance for Brugada syndrome 1

Included ClinVar conditions (24):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_001040151.2(SCN3B):c.29T>C (p.Leu10Pro) rs121918282 0.00036
NM_001040151.2(SCN3B):c.*4588T>C rs765294617 0.00006
NM_001040151.2(SCN3B):c.*2366G>A rs867302682 0.00004
NM_001040151.2(SCN3B):c.-326C>G rs886047906 0.00001
NM_001040151.2(SCN3B):c.*1007dup rs72553907
NM_001040151.2(SCN3B):c.*1948TATT[2] rs776449566
NM_001040151.2(SCN3B):c.*2795GAA[1] rs544984224
NM_001040151.2(SCN3B):c.*447C>A rs80017720
NM_001040151.2(SCN3B):c.-62del rs886047904
NM_001040151.2(SCN3B):c.118C>T (p.Pro40Ser) rs762633602

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