Have questions? Visit https://www.reddit.com/r/SNPedia

rs7255066

From SNPedia

Orientationplus
Stabilizedplus
Make rs7255066(C;C)
Make rs7255066(C;T)
Make rs7255066(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position44642803
GenePVR
is asnp
is mentioned by
dbSNPrs7255066
ebirs7255066
HLIrs7255066
Exacrs7255066
Varsomers7255066
Maprs7255066
PheGenIrs7255066
hapmaprs7255066
1000 genomesrs7255066
hgdprs7255066
ensemblrs7255066
gopubmedrs7255066
geneviewrs7255066
scholarrs7255066
googlers7255066
pharmgkbrs7255066
gwascentralrs7255066
openSNPrs7255066
23andMers7255066
23andMe allrs7255066
SNP Nexus

SNPshotrs7255066
SNPdbers7255066
MSV3drs7255066
GWAS Ctlgrs7255066
GMAF0.4614
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 0.000001
Odds Ratio 1.0900 [1.07-1.11]