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rs4669226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs4669226(A;G)
Make rs4669226(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position7913466
is asnp
is mentioned by
dbSNPrs4669226
ebirs4669226
HLIrs4669226
Exacrs4669226
Varsomers4669226
Maprs4669226
PheGenIrs4669226
hapmaprs4669226
1000 genomesrs4669226
hgdprs4669226
ensemblrs4669226
gopubmedrs4669226
geneviewrs4669226
scholarrs4669226
googlers4669226
pharmgkbrs4669226
gwascentralrs4669226
openSNPrs4669226
23andMers4669226
23andMe allrs4669226
SNP Nexus

SNPshotrs4669226
SNPdbers4669226
MSV3drs4669226
GWAS Ctlgrs4669226
GMAF0.03994
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23412934OA-icon.png]
Trait Multiple sclerosis
Title A genome-wide association study of brain lesion distribution in multiple sclerosis.
Risk Allele
P-val 5E-6
Odds Ratio NR NR