Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1565214594
rs1565214594
NFKB2 ; PSD
C 0.700 GeneticVariation CLINVAR Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency. 24140114

2013
dbSNP: rs1565214594
rs1565214594
NFKB2 ; PSD
C 0.700 GeneticVariation CLINVAR beta-TrCP binding and processing of NF-kappaB2/p100 involve its phosphorylation at serines 866 and 870. 16303288

2006