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rs8112449

From SNPedia

Orientationplus
Stabilizedplus
Make rs8112449(A;A)
Make rs8112449(A;G)
Make rs8112449(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10409388
is asnp
is mentioned by
dbSNPrs8112449
ebirs8112449
HLIrs8112449
Exacrs8112449
Varsomers8112449
Maprs8112449
PheGenIrs8112449
hapmaprs8112449
1000 genomesrs8112449
hgdprs8112449
ensemblrs8112449
gopubmedrs8112449
geneviewrs8112449
scholarrs8112449
googlers8112449
pharmgkbrs8112449
gwascentralrs8112449
openSNPrs8112449
23andMers8112449
23andMe allrs8112449
SNP Nexus

SNPshotrs8112449
SNPdbers8112449
MSV3drs8112449
GWAS Ctlgrs8112449
GMAF0.3512
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait Multiple sclerosis
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele G
P-val 1E-6
Odds Ratio 1.08 [1.07-1.1]