List of variants in gene TNFRSF13B reported by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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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.145T>C (p.Ser49Pro)	rs374547688	0.00023
NM_012452.3(TNFRSF13B):c.592C>T (p.Arg198Cys)	rs140781824	0.00016
NM_012452.3(TNFRSF13B):c.34C>T (p.Arg12Trp)	rs779924436	0.00006

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