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rs11026091

From SNPedia

Orientationplus
Stabilizedplus
Make rs11026091(A;A)
Make rs11026091(A;G)
Make rs11026091(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position3238579
is asnp
is mentioned by
dbSNPrs11026091
dbSNP (classic)rs11026091
ClinGenrs11026091
ebirs11026091
HLIrs11026091
Exacrs11026091
Gnomadrs11026091
Varsomers11026091
LitVarrs11026091
Maprs11026091
PheGenIrs11026091
Biobankrs11026091
1000 genomesrs11026091
hgdprs11026091
ensemblrs11026091
geneviewrs11026091
scholarrs11026091
googlers11026091
pharmgkbrs11026091
gwascentralrs11026091
openSNPrs11026091
23andMers11026091
SNPshotrs11026091
SNPdbers11026091
MSV3drs11026091
GWAS Ctlgrs11026091
GMAF0.4835
Max Magnitude0
? (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 2E-6
Odds Ratio NR NR