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rs397514331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514331(-;-)
Make rs397514331(-;A)
ReferenceGRCh38 38.1/142
Chromosome10
Position102402144
GeneNFKB2, PSD
is asnp
is mentioned by
dbSNPrs397514331
dbSNP (old)rs397514331
ClinGenrs397514331
ebirs397514331
HLIrs397514331
Exacrs397514331
Gnomadrs397514331
Varsomers397514331
Maprs397514331
PheGenIrs397514331
Biobankrs397514331
1000 genomesrs397514331
hgdprs397514331
ensemblrs397514331
gopubmedrs397514331
geneviewrs397514331
scholarrs397514331
googlers397514331
pharmgkbrs397514331
gwascentralrs397514331
openSNPrs397514331
23andMers397514331
23andMe allrs397514331
SNP Nexus

SNPshotrs397514331
SNPdbers397514331
MSV3drs397514331
GWAS Ctlgrs397514331
Max Magnitude0
ClinVar
Risk rs397514331(-;-)
Alt rs397514331(-;-)
Reference Rs397514331(A;A)
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.104161902delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000055613.1, RCV000077760.3,