ClinVar Miner

List of variants reported as pathogenic for Immunodeficiency, common variable, 2 by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg)	rs34557412	0.00403
NM_012452.2(TNFRSF13B):c.581_582delCCinsAA (p.Ser194Ter)	rs121908379

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