Have questions? Visit https://www.reddit.com/r/SNPedia

rs727502788

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727502788(C;T)
Make rs727502788(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position102402273
GeneNFKB2, PSD
is asnp
is mentioned by
dbSNPrs727502788
ebirs727502788
HLIrs727502788
Exacrs727502788
Varsomers727502788
Maprs727502788
PheGenIrs727502788
hapmaprs727502788
1000 genomesrs727502788
hgdprs727502788
ensemblrs727502788
gopubmedrs727502788
geneviewrs727502788
scholarrs727502788
googlers727502788
pharmgkbrs727502788
gwascentralrs727502788
openSNPrs727502788
23andMers727502788
23andMe allrs727502788
SNP Nexus

SNPshotrs727502788
SNPdbers727502788
MSV3drs727502788
GWAS Ctlgrs727502788
Max Magnitude0
ClinVar
Risk rs727502788(T;T)
Alt rs727502788(T;T)
Reference Rs727502788(C;C)
Significance Pathogenic
Disease Common variable immunodeficiency 10
Variation info
Gene PSD NFKB2
CLNDBN Common variable immunodeficiency 10
Reversed 0
HGVS NC_000010.10:g.104162030C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000150033.3,