ClinVar Miner

List of variants in gene TNFRSF13C reported as benign for agammaglobulinemia

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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NM_052945.3(TNFRSF13C):c.*120T>C rs7290134
NM_052945.3(TNFRSF13C):c.191G>T (p.Gly64Val) rs547352394
NM_052945.3(TNFRSF13C):c.191_192delinsTT (p.Gly64Val) rs1556157858
NM_052945.3(TNFRSF13C):c.192C>T (p.Gly64=) rs529563231
NM_052945.3(TNFRSF13C):c.229C>T (p.Leu77=) rs140820836
NM_052945.3(TNFRSF13C):c.246C>T (p.Pro82=) rs779365266
NM_052945.3(TNFRSF13C):c.282C>T (p.Val94=) rs190252814
NM_052945.3(TNFRSF13C):c.60C>T (p.Val20=) rs373828157
NM_052945.3(TNFRSF13C):c.62C>G (p.Pro21Arg) rs77874543

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