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rs397514332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514332(C;T)
Make rs397514332(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position102402138
GeneNFKB2, PSD
is asnp
is mentioned by
dbSNPrs397514332
ebirs397514332
HLIrs397514332
Exacrs397514332
Varsomers397514332
Maprs397514332
PheGenIrs397514332
hapmaprs397514332
1000 genomesrs397514332
hgdprs397514332
ensemblrs397514332
gopubmedrs397514332
geneviewrs397514332
scholarrs397514332
googlers397514332
pharmgkbrs397514332
gwascentralrs397514332
openSNPrs397514332
23andMers397514332
23andMe allrs397514332
SNP Nexus

SNPshotrs397514332
SNPdbers397514332
MSV3drs397514332
GWAS Ctlgrs397514332
Max Magnitude0
ClinVar
Risk rs397514332(T;T)
Alt rs397514332(T;T)
Reference rs397514332(C;C)
Significance Pathogenic
Disease Common variable immunodeficiency 1 Common variable immunodeficiency 10
Variation info
Gene PSD NFKB2
CLNDBN Common variable immunodeficiency 1 Common variable immunodeficiency 10
Reversed 0
HGVS NC_000010.10:g.104161895C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000055612.1, RCV000077761.4,