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rs3091315

From SNPedia

Orientationplus
Stabilizedplus
Make rs3091315(A;A)
Make rs3091315(A;G)
Make rs3091315(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position34266646
is asnp
is mentioned by
dbSNPrs3091315
ebirs3091315
HLIrs3091315
Exacrs3091315
Varsomers3091315
Maprs3091315
PheGenIrs3091315
hapmaprs3091315
1000 genomesrs3091315
hgdprs3091315
ensemblrs3091315
gopubmedrs3091315
geneviewrs3091315
scholarrs3091315
googlers3091315
pharmgkbrs3091315
gwascentralrs3091315
openSNPrs3091315
23andMers3091315
23andMe allrs3091315
SNP Nexus

SNPshotrs3091315
SNPdbers3091315
MSV3drs3091315
GWAS Ctlgrs3091315
GMAF0.4463
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Risk Allele A
P-val 2E-13
Odds Ratio 1.2000 [1.14-1.26]