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rs9321490

From SNPedia

Orientationplus
Stabilizedplus
Make rs9321490(C;C)
Make rs9321490(C;T)
Make rs9321490(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position135173737
is asnp
is mentioned by
dbSNPrs9321490
ebirs9321490
HLIrs9321490
Exacrs9321490
Varsomers9321490
Maprs9321490
PheGenIrs9321490
hapmaprs9321490
1000 genomesrs9321490
hgdprs9321490
ensemblrs9321490
gopubmedrs9321490
geneviewrs9321490
scholarrs9321490
googlers9321490
pharmgkbrs9321490
gwascentralrs9321490
openSNPrs9321490
23andMers9321490
23andMe allrs9321490
SNP Nexus

SNPshotrs9321490
SNPdbers9321490
MSV3drs9321490
GWAS Ctlgrs9321490
GMAF0.2971
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 G
P-val 0.000002
Odds Ratio 1.1000 [1.08-1.11]