ClinVar Miner

List of variants in gene TNFRSF13C reported as likely benign for agammaglobulinemia

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_052945.3(TNFRSF13C):c.132A>G (p.Lys44=) rs920471641
NM_052945.3(TNFRSF13C):c.137-7delG rs1299671576
NM_052945.3(TNFRSF13C):c.213G>A (p.Ala71=) rs767759337
NM_052945.3(TNFRSF13C):c.264A>G (p.Ala88=) rs778024793
NM_052945.3(TNFRSF13C):c.317G>A (p.Arg106Gln) rs150374940
NM_052945.3(TNFRSF13C):c.367+10G>T rs1052448266
NM_052945.3(TNFRSF13C):c.475C>T (p.His159Tyr) rs61756766

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