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rs3091316

From SNPedia

Orientationplus
Stabilizedplus
Make rs3091316(A;A)
Make rs3091316(A;G)
Make rs3091316(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position34266955
is asnp
is mentioned by
dbSNPrs3091316
dbSNP (classic)rs3091316
ClinGenrs3091316
ebirs3091316
HLIrs3091316
Exacrs3091316
Gnomadrs3091316
Varsomers3091316
LitVarrs3091316
Maprs3091316
PheGenIrs3091316
Biobankrs3091316
1000 genomesrs3091316
hgdprs3091316
ensemblrs3091316
geneviewrs3091316
scholarrs3091316
googlers3091316
pharmgkbrs3091316
gwascentralrs3091316
openSNPrs3091316
23andMers3091316
SNPshotrs3091316
SNPdbers3091316
MSV3drs3091316
GWAS Ctlgrs3091316
GMAF0.41
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22412388OA-icon.png]
Trait
Title A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.
Risk Allele G
P-val 4E-8
Odds Ratio 1.1400 None
GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Inflammatory bowel disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele G
P-val 1E-26
Odds Ratio 1.12 [1.087-1.158]