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rs17594362

From SNPedia

Orientationplus
Stabilizedplus
Make rs17594362(C;C)
Make rs17594362(C;T)
Make rs17594362(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position41565109
is asnp
is mentioned by
dbSNPrs17594362
ebirs17594362
HLIrs17594362
Exacrs17594362
Varsomers17594362
Maprs17594362
PheGenIrs17594362
hapmaprs17594362
1000 genomesrs17594362
hgdprs17594362
ensemblrs17594362
gopubmedrs17594362
geneviewrs17594362
scholarrs17594362
googlers17594362
pharmgkbrs17594362
gwascentralrs17594362
openSNPrs17594362
23andMers17594362
23andMe allrs17594362
SNP Nexus

SNPshotrs17594362
SNPdbers17594362
MSV3drs17594362
GWAS Ctlgrs17594362
GMAF0.1625
Max Magnitude
? (C;C) (C;T) (T;T) 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 A
P-val 4E-6
Odds Ratio 1.11 [1.09-1.13]