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rs11129295

From SNPedia

Orientationplus
Stabilizedplus
Make rs11129295(C;C)
Make rs11129295(C;T)
Make rs11129295(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position27747289
is asnp
is mentioned by
dbSNPrs11129295
ebirs11129295
HLIrs11129295
Exacrs11129295
Varsomers11129295
Maprs11129295
PheGenIrs11129295
hapmaprs11129295
1000 genomesrs11129295
hgdprs11129295
ensemblrs11129295
gopubmedrs11129295
geneviewrs11129295
scholarrs11129295
googlers11129295
pharmgkbrs11129295
gwascentralrs11129295
openSNPrs11129295
23andMers11129295
23andMe allrs11129295
SNP Nexus

SNPshotrs11129295
SNPdbers11129295
MSV3drs11129295
GWAS Ctlgrs11129295
GMAF0.494
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele A
P-val 1E-9
Odds Ratio 1.1100 [1.09-1.12]