ClinVar Miner

List of variants in gene TNFRSF13B reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_012452.3(TNFRSF13B):c.61+67del rs1423111679 0.00003
NM_012452.3(TNFRSF13B):c.11T>C (p.Leu4Pro) rs2087749301 0.00001
NM_012452.3(TNFRSF13B):c.632-2A>G

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