ClinVar Miner

List of variants in gene NFKB2 reported as benign for B cell deficiency

Included ClinVar conditions (64):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001322934.2(NFKB2):c.1821A>G (p.Ala607=) rs4919634 0.99720
NM_001322934.2(NFKB2):c.2467-9T>A rs11574853 0.05268
NM_001322934.2(NFKB2):c.2094C>T (p.Asn698=) rs11574851 0.03687
NM_001322934.2(NFKB2):c.2239C>T (p.Leu747=) rs11191279 0.01026
NM_001322934.2(NFKB2):c.1869G>A (p.Gly623=) rs138786808 0.00361
NM_001322934.2(NFKB2):c.21+13G>A rs199513883 0.00288
NM_001322934.2(NFKB2):c.1821= (p.Ala607=) rs4919634 0.00280
NM_001322934.2(NFKB2):c.1962C>T (p.Val654=) rs201623844 0.00221
NM_001322934.2(NFKB2):c.1826G>A (p.Arg609Gln) rs200092317 0.00151
NM_001322934.2(NFKB2):c.2145G>A (p.Ser715=) rs200006038 0.00128
NM_001322934.2(NFKB2):c.2224-15C>T rs142623210 0.00125
NM_001322934.2(NFKB2):c.1608C>A (p.Ile536=) rs34916280 0.00083
NM_001322934.2(NFKB2):c.921G>A (p.Leu307=) rs146926941 0.00064
NM_001322934.2(NFKB2):c.2224-10G>A rs550812736 0.00034
NM_001322934.2(NFKB2):c.1117+7G>T rs188346889 0.00026
NM_001322934.2(NFKB2):c.1953C>G (p.Thr651=) rs372873787 0.00022
NM_001322934.2(NFKB2):c.978C>T (p.Tyr326=) rs2295587 0.00016
NM_001322934.2(NFKB2):c.243+20G>C rs371813362 0.00014
NM_001322934.2(NFKB2):c.1539C>T (p.His513=) rs533142885 0.00010
NM_001322934.2(NFKB2):c.503-16T>C rs201456641 0.00009
NM_001322934.2(NFKB2):c.2475C>T (p.Gly825=) rs200482499 0.00008
NM_001322934.2(NFKB2):c.1969-17G>A rs375150780 0.00006
NM_001322934.2(NFKB2):c.503-17A>G rs201960564 0.00006
NM_001322934.2(NFKB2):c.767-13G>A rs746075690 0.00004
NM_001322934.2(NFKB2):c.853-8C>A rs749266689 0.00003
NM_001322934.2(NFKB2):c.1584+11G>A
NM_001322934.2(NFKB2):c.1584+9dup rs935753166
NM_001322934.2(NFKB2):c.1821A>C (p.Ala607=)
NM_001322934.2(NFKB2):c.502+16dup
NM_001322934.2(NFKB2):c.502+22_502+45del

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.