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rs771767

From SNPedia

Orientationminus
Stabilizedplus
Make rs771767(C;C)
Make rs771767(C;T)
Make rs771767(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position102029794
is asnp
is mentioned by
dbSNPrs771767
ebirs771767
HLIrs771767
Exacrs771767
Varsomers771767
Maprs771767
PheGenIrs771767
hapmaprs771767
1000 genomesrs771767
hgdprs771767
ensemblrs771767
gopubmedrs771767
geneviewrs771767
scholarrs771767
googlers771767
pharmgkbrs771767
gwascentralrs771767
openSNPrs771767
23andMers771767
23andMe allrs771767
SNP Nexus

SNPshotrs771767
SNPdbers771767
MSV3drs771767
GWAS Ctlgrs771767
GMAF0.225
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 9E-9
Odds Ratio 1.1000 [1.09-1.12]