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rs7714584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7714584(A;G)
Make rs7714584(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150890858
is asnp
is mentioned by
dbSNPrs7714584
ebirs7714584
HLIrs7714584
Exacrs7714584
Varsomers7714584
Maprs7714584
PheGenIrs7714584
hapmaprs7714584
1000 genomesrs7714584
hgdprs7714584
ensemblrs7714584
gopubmedrs7714584
geneviewrs7714584
scholarrs7714584
googlers7714584
pharmgkbrs7714584
gwascentralrs7714584
openSNPrs7714584
23andMers7714584
23andMe allrs7714584
SNP Nexus

SNPshotrs7714584
SNPdbers7714584
MSV3drs7714584
GWAS Ctlgrs7714584
GMAF0.2828
Max Magnitude0
? (A;A) (A;G) (G;G) 28
23andMe blog rs7714584(G) linked with an increased risk for Crohn's disease. Similar to rs13361189
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 G
P-val 8E-19
Odds Ratio 1.3700 [1.28-1.47]