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rs869320689

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869320689(G;G)
Make rs869320689(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position102580641
GeneLOC101929401, NFKB1
is asnp
is mentioned by
dbSNPrs869320689
ebirs869320689
HLIrs869320689
Exacrs869320689
Varsomers869320689
Maprs869320689
PheGenIrs869320689
hapmaprs869320689
1000 genomesrs869320689
hgdprs869320689
ensemblrs869320689
gopubmedrs869320689
geneviewrs869320689
scholarrs869320689
googlers869320689
pharmgkbrs869320689
gwascentralrs869320689
openSNPrs869320689
23andMers869320689
23andMe allrs869320689
SNP Nexus

SNPshotrs869320689
SNPdbers869320689
MSV3drs869320689
GWAS Ctlgrs869320689
Max Magnitude0
ClinVar
Risk rs869320689(G;G)
Alt rs869320689(G;G)
Reference rs869320689(T;T)
Significance Pathogenic
Disease Immunodeficiency
Variation info
Gene NFKB1
CLNDBN Immunodeficiency, common variable, 12
Reversed 0
HGVS NC_000004.11:g.103501798T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000194108.3,