Have questions? Visit https://www.reddit.com/r/SNPedia

rs4902642

From SNPedia

Orientationplus
Stabilizedplus
Make rs4902642(A;A)
Make rs4902642(A;G)
Make rs4902642(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position68743482
is asnp
is mentioned by
dbSNPrs4902642
ebirs4902642
HLIrs4902642
Exacrs4902642
Varsomers4902642
Maprs4902642
PheGenIrs4902642
hapmaprs4902642
1000 genomesrs4902642
hgdprs4902642
ensemblrs4902642
gopubmedrs4902642
geneviewrs4902642
scholarrs4902642
googlers4902642
pharmgkbrs4902642
gwascentralrs4902642
openSNPrs4902642
23andMers4902642
23andMe allrs4902642
SNP Nexus

SNPshotrs4902642
SNPdbers4902642
MSV3drs4902642
GWAS Ctlgrs4902642
GMAF0.3283
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 G
P-val 2E-10
Odds Ratio 1.0700 [1.11-1.04]