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rs869320754

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs869320754(-;A)
Make rs869320754(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position102576933
GeneNFKB1
is asnp
is mentioned by
dbSNPrs869320754
dbSNP (classic)rs869320754
ClinGenrs869320754
ebirs869320754
HLIrs869320754
Exacrs869320754
Gnomadrs869320754
Varsomers869320754
LitVarrs869320754
Maprs869320754
PheGenIrs869320754
Biobankrs869320754
1000 genomesrs869320754
hgdprs869320754
ensemblrs869320754
geneviewrs869320754
scholarrs869320754
googlers869320754
pharmgkbrs869320754
gwascentralrs869320754
openSNPrs869320754
23andMers869320754
SNPshotrs869320754
SNPdbers869320754
MSV3drs869320754
GWAS Ctlgrs869320754
Max Magnitude0
ClinVar
Risk rs869320754(A;A)
Alt rs869320754(A;A)
Reference Rs869320754(-;-)
Significance Pathogenic
Disease Immunodeficiency
Variation info
Gene NFKB1 LOC101929401
CLNDBN Immunodeficiency, common variable, 12
Reversed 0
HGVS NC_000004.11:g.103498090dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000195130.2,