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rs713875

From SNPedia

Orientationplus
Stabilizedplus
Make rs713875(C;C)
Make rs713875(C;G)
Make rs713875(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position30196498
is asnp
is mentioned by
dbSNPrs713875
ebirs713875
HLIrs713875
Exacrs713875
Varsomers713875
Maprs713875
PheGenIrs713875
hapmaprs713875
1000 genomesrs713875
hgdprs713875
ensemblrs713875
gopubmedrs713875
geneviewrs713875
scholarrs713875
googlers713875
pharmgkbrs713875
gwascentralrs713875
openSNPrs713875
23andMers713875
23andMe allrs713875
SNP Nexus

SNPshotrs713875
SNPdbers713875
MSV3drs713875
GWAS Ctlgrs713875
GMAF0.483
Max Magnitude
? (C;C) (C;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 C
P-val 7E-12
Odds Ratio 1.0800 [1.04-1.13]