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rs12242110

From SNPedia

Orientationplus
Stabilizedplus
Make rs12242110(A;A)
Make rs12242110(A;G)
Make rs12242110(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position35246767
GeneCCNY
is asnp
is mentioned by
dbSNPrs12242110
ebirs12242110
HLIrs12242110
Exacrs12242110
Varsomers12242110
Maprs12242110
PheGenIrs12242110
hapmaprs12242110
1000 genomesrs12242110
hgdprs12242110
ensemblrs12242110
gopubmedrs12242110
geneviewrs12242110
scholarrs12242110
googlers12242110
pharmgkbrs12242110
gwascentralrs12242110
openSNPrs12242110
23andMers12242110
23andMe allrs12242110
SNP Nexus

SNPshotrs12242110
SNPdbers12242110
MSV3drs12242110
GWAS Ctlgrs12242110
GMAF0.3287
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 1E-9
Odds Ratio 1.15 [1.10-1.20]