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rs4271113

From SNPedia

Orientationplus
Stabilizedplus
Make rs4271113(A;A)
Make rs4271113(A;G)
Make rs4271113(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position34874386
is asnp
is mentioned by
dbSNPrs4271113
ebirs4271113
HLIrs4271113
Exacrs4271113
Varsomers4271113
Maprs4271113
PheGenIrs4271113
hapmaprs4271113
1000 genomesrs4271113
hgdprs4271113
ensemblrs4271113
gopubmedrs4271113
geneviewrs4271113
scholarrs4271113
googlers4271113
pharmgkbrs4271113
gwascentralrs4271113
openSNPrs4271113
23andMers4271113
23andMe allrs4271113
SNP Nexus

SNPshotrs4271113
SNPdbers4271113
MSV3drs4271113
GWAS Ctlgrs4271113
GMAF0.2461
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23412934OA-icon.png]
Trait Multiple sclerosis
Title A genome-wide association study of brain lesion distribution in multiple sclerosis.
Risk Allele
P-val 9E-7
Odds Ratio NR NR