List of variants in gene TNFRSF13B studied for Immunodeficiency, common variable, 2; Immunoglobulin A deficiency 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_012452.3(TNFRSF13B):c.542C>A (p.Ala181Glu)	rs72553883	0.00518
NM_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg)	rs34557412	0.00403
NM_012452.3(TNFRSF13B):c.215G>A (p.Arg72His)	rs55916807	0.00261
NM_012452.3(TNFRSF13B):c.204dup (p.Leu69fs)	rs72553875	0.00031
NM_012452.3(TNFRSF13B):c.641T>C (p.Met214Thr)	rs144560464	0.00027
NM_012452.3(TNFRSF13B):c.145T>C (p.Ser49Pro)	rs374547688	0.00023
NM_012452.3(TNFRSF13B):c.592C>T (p.Arg198Cys)	rs140781824	0.00016
NM_012452.3(TNFRSF13B):c.58C>T (p.Arg20Cys)	rs200013015	0.00012
NM_012452.3(TNFRSF13B):c.706G>T (p.Glu236Ter)	rs201021960	0.00010
NM_012452.3(TNFRSF13B):c.34C>T (p.Arg12Trp)	rs779924436	0.00006
NM_012452.3(TNFRSF13B):c.214C>T (p.Arg72Cys)	rs375514495	0.00004
NM_012452.3(TNFRSF13B):c.693C>G (p.Ser231Arg)	rs145711865	0.00003
NM_012452.3(TNFRSF13B):c.53A>G (p.Glu18Gly)	rs1597672265
NM_012452.3(TNFRSF13B):c.61+1G>A	rs1016142312

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