ClinVar Miner

List of variants in gene combination TNFSF12, TNFSF12-TNFSF13 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: 3
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HGVS dbSNP
NM_003809.2(TNFSF12):c.498+9delC rs1356188583
NM_003809.3(TNFSF12):c.42G>A (p.Gly14=) rs1170763703
NM_003809.3(TNFSF12):c.450C>T (p.Ile150=) rs147597489

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