ClinVar Miner

List of variants in gene TNFRSF13B reported as likely pathogenic for agammaglobulinemia

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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NM_012452.2(TNFRSF13B):c.204dup (p.Leu69fs) rs72553875
NM_012452.2(TNFRSF13B):c.310T>C (p.Cys104Arg) rs34557412
NM_012452.2(TNFRSF13B):c.311G>A (p.Cys104Tyr) rs72553879
NM_012452.2(TNFRSF13B):c.542C>A (p.Ala181Glu) rs72553883

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