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

rs4939490

From SNPedia

Orientationplus
Stabilizedplus
Make rs4939490(C;C)
Make rs4939490(C;G)
Make rs4939490(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position61026179
is asnp
is mentioned by
dbSNPrs4939490
ebirs4939490
HLIrs4939490
Exacrs4939490
Varsomers4939490
Maprs4939490
PheGenIrs4939490
hapmaprs4939490
1000 genomesrs4939490
hgdprs4939490
ensemblrs4939490
gopubmedrs4939490
geneviewrs4939490
scholarrs4939490
googlers4939490
pharmgkbrs4939490
gwascentralrs4939490
openSNPrs4939490
23andMers4939490
23andMe allrs4939490
SNP Nexus

SNPshotrs4939490
SNPdbers4939490
MSV3drs4939490
GWAS Ctlgrs4939490
GMAF0.3765
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21244703OA-icon.png]
Trait
Title Modeling the Cumulative Genetic Risk for Multiple Sclerosis from Genome Wide Association Data
Risk Allele
P-val 1E-9
Odds Ratio 1.3000 [1.19-1.42]