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rs727502787

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727502787(A;G)
Make rs727502787(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position102402267
GeneNFKB2, PSD
is asnp
is mentioned by
dbSNPrs727502787
ebirs727502787
HLIrs727502787
Exacrs727502787
Varsomers727502787
Maprs727502787
PheGenIrs727502787
hapmaprs727502787
1000 genomesrs727502787
hgdprs727502787
ensemblrs727502787
gopubmedrs727502787
geneviewrs727502787
scholarrs727502787
googlers727502787
pharmgkbrs727502787
gwascentralrs727502787
openSNPrs727502787
23andMers727502787
23andMe allrs727502787
SNP Nexus

SNPshotrs727502787
SNPdbers727502787
MSV3drs727502787
GWAS Ctlgrs727502787
Max Magnitude0
ClinVar
Risk rs727502787(G;G)
Alt rs727502787(G;G)
Reference rs727502787(A;A)
Significance Pathogenic
Disease Common variable immunodeficiency 10
Variation info
Gene PSD NFKB2
CLNDBN Common variable immunodeficiency 10
Reversed 0
HGVS NC_000010.10:g.104162024A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000150032.3,