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rs7927997

From SNPedia

Orientationplus
Stabilizedplus
Make rs7927997(C;C)
Make rs7927997(C;T)
Make rs7927997(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position76590331
is asnp
is mentioned by
dbSNPrs7927997
ebirs7927997
HLIrs7927997
Exacrs7927997
Varsomers7927997
Maprs7927997
PheGenIrs7927997
hapmaprs7927997
1000 genomesrs7927997
hgdprs7927997
ensemblrs7927997
gopubmedrs7927997
geneviewrs7927997
scholarrs7927997
googlers7927997
pharmgkbrs7927997
gwascentralrs7927997
openSNPrs7927997
23andMers7927997
23andMe allrs7927997
SNP Nexus

SNPshotrs7927997
SNPdbers7927997
MSV3drs7927997
GWAS Ctlgrs7927997
GMAF0.2723
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait Crohn's disease
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Risk Allele T
P-val 6E-13
Odds Ratio 1.17 [1.12-1.22]