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rs13073817

From SNPedia

Orientationplus
Stabilizedplus
Make rs13073817(A;A)
Make rs13073817(A;G)
Make rs13073817(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position18665366
is asnp
is mentioned by
dbSNPrs13073817
ebirs13073817
HLIrs13073817
Exacrs13073817
Varsomers13073817
Maprs13073817
PheGenIrs13073817
hapmaprs13073817
1000 genomesrs13073817
hgdprs13073817
ensemblrs13073817
gopubmedrs13073817
geneviewrs13073817
scholarrs13073817
googlers13073817
pharmgkbrs13073817
gwascentralrs13073817
openSNPrs13073817
23andMers13073817
23andMe allrs13073817
SNP Nexus

SNPshotrs13073817
SNPdbers13073817
MSV3drs13073817
GWAS Ctlgrs13073817
GMAF0.185
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 7E-9
Odds Ratio 1.0800 [1.03-1.13]