ClinVar Miner

List of variants in gene TNFRSF13B reported as 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_012452.2(TNFRSF13B):c.291T>G (p.Pro97=) rs35062843
NM_012452.2(TNFRSF13B):c.560_562AGA[1] (p.Lys188del) rs376630110
NM_012452.2(TNFRSF13B):c.563A>T (p.Lys188Met) rs74811083
NM_012452.2(TNFRSF13B):c.605G>A (p.Arg202His) rs104894649
NM_012452.2(TNFRSF13B):c.61+10C>T rs148297590
NM_012452.2(TNFRSF13B):c.659T>C (p.Val220Ala) rs56063729
NM_012452.2(TNFRSF13B):c.81G>A (p.Thr27=) rs8072293

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