ClinVar Miner

List of variants in gene NFKB2 reported as likely benign for agammaglobulinemia

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_001077494.3(NFKB2):c.1170C>A (p.Ser390=) rs1200632324
NM_001077494.3(NFKB2):c.1288C>T (p.Pro430Ser) rs202001697
NM_001077494.3(NFKB2):c.1386C>G (p.Leu462=) rs762807587
NM_001077494.3(NFKB2):c.1736G>A (p.Arg579His) rs200227171
NM_001077494.3(NFKB2):c.2072-3C>T rs201550645
NM_001077494.3(NFKB2):c.2167G>A (p.Asp723Asn) rs199577673
NM_001077494.3(NFKB2):c.216G>A (p.Lys72=) rs369551276
NM_001077494.3(NFKB2):c.2286C>T (p.Ser762=) rs899733509
NM_001077494.3(NFKB2):c.2418G>A (p.Thr806=) rs1488705625
NM_001077494.3(NFKB2):c.2601G>A (p.Ala867=) rs1438477157
NM_001077494.3(NFKB2):c.396-5C>T rs373971415

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.