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

rs4792814

From SNPedia

Orientationplus
Stabilizedplus
Make rs4792814(C;C)
Make rs4792814(C;T)
Make rs4792814(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position45325639
is asnp
is mentioned by
dbSNPrs4792814
ebirs4792814
HLIrs4792814
Exacrs4792814
Varsomers4792814
Maprs4792814
PheGenIrs4792814
hapmaprs4792814
1000 genomesrs4792814
hgdprs4792814
ensemblrs4792814
gopubmedrs4792814
geneviewrs4792814
scholarrs4792814
googlers4792814
pharmgkbrs4792814
gwascentralrs4792814
openSNPrs4792814
23andMers4792814
23andMe allrs4792814
SNP Nexus

SNPshotrs4792814
SNPdbers4792814
MSV3drs4792814
GWAS Ctlgrs4792814
GMAF0.4004
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 G
P-val 3E-6
Odds Ratio 1.08 [1.06-1.09]