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rs869320688

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869320688(A;G)
Make rs869320688(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position102579043
GeneLOC101929401, NFKB1
is asnp
is mentioned by
dbSNPrs869320688
ebirs869320688
HLIrs869320688
Exacrs869320688
Varsomers869320688
Maprs869320688
PheGenIrs869320688
hapmaprs869320688
1000 genomesrs869320688
hgdprs869320688
ensemblrs869320688
gopubmedrs869320688
geneviewrs869320688
scholarrs869320688
googlers869320688
pharmgkbrs869320688
gwascentralrs869320688
openSNPrs869320688
23andMers869320688
23andMe allrs869320688
SNP Nexus

SNPshotrs869320688
SNPdbers869320688
MSV3drs869320688
GWAS Ctlgrs869320688
Max Magnitude0
ClinVar
Risk rs869320688(G;G)
Alt rs869320688(G;G)
Reference rs869320688(A;A)
Significance Pathogenic
Disease Immunodeficiency
Variation info
Gene NFKB1 LOC101929401
CLNDBN Immunodeficiency, common variable, 12
Reversed 0
HGVS NC_000004.11:g.103500200A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000192693.3,