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rs11117432

From SNPedia

Orientationplus
Stabilizedplus
Make rs11117432(A;A)
Make rs11117432(A;G)
Make rs11117432(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position85985665
is asnp
is mentioned by
dbSNPrs11117432
dbSNP (classic)rs11117432
ClinGenrs11117432
ebirs11117432
HLIrs11117432
Exacrs11117432
Gnomadrs11117432
Varsomers11117432
LitVarrs11117432
Maprs11117432
PheGenIrs11117432
Biobankrs11117432
1000 genomesrs11117432
hgdprs11117432
ensemblrs11117432
geneviewrs11117432
scholarrs11117432
googlers11117432
pharmgkbrs11117432
gwascentralrs11117432
openSNPrs11117432
23andMers11117432
SNPshotrs11117432
SNPdbers11117432
MSV3drs11117432
GWAS Ctlgrs11117432
GMAF0.1295
Max Magnitude0
? (A;A) (A;G) (G;G) 28


DeCode reports that rs11117432 is associated with risk of multiple sclerosis. [PMID 19525953OA-icon.png]

GWAS snp
PMID [PMID 21399635OA-icon.png]
Trait
Title Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
Risk Allele G
P-val 5E-11
Odds Ratio 1.3100 [1.21-1.43]