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rs7702331

From SNPedia

Orientationplus
Stabilizedplus
Make rs7702331(A;A)
Make rs7702331(A;G)
Make rs7702331(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position73255307
is asnp
is mentioned by
dbSNPrs7702331
ebirs7702331
HLIrs7702331
Exacrs7702331
Varsomers7702331
Maprs7702331
PheGenIrs7702331
hapmaprs7702331
1000 genomesrs7702331
hgdprs7702331
ensemblrs7702331
gopubmedrs7702331
geneviewrs7702331
scholarrs7702331
googlers7702331
pharmgkbrs7702331
gwascentralrs7702331
openSNPrs7702331
23andMers7702331
23andMe allrs7702331
SNP Nexus

SNPshotrs7702331
SNPdbers7702331
MSV3drs7702331
GWAS Ctlgrs7702331
GMAF0.3485
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 6E-12
Odds Ratio 1.1200 [1.07-1.17]
GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Crohn's disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele A
P-val 6E-10
Odds Ratio 1.09 [1.05-1.126]