ClinVar Miner

List of variants reported as pathogenic for immunodeficiency, common variable, 1 by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012452.3(TNFRSF13B):c.310T>C (p.Cys104Arg)	rs34557412	0.00403
NM_001322934.2(NFKB2):c.2557C>T (p.Arg853Ter)	rs397514332

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