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rs1736020

From SNPedia

Orientationplus
Stabilizedplus
Make rs1736020(A;A)
Make rs1736020(A;C)
Make rs1736020(C;C)
ReferenceGRCh38 38.1/141
Chromosome21
Position15440233
is asnp
is mentioned by
dbSNPrs1736020
ebirs1736020
HLIrs1736020
Exacrs1736020
Varsomers1736020
Maprs1736020
PheGenIrs1736020
hapmaprs1736020
1000 genomesrs1736020
hgdprs1736020
ensemblrs1736020
gopubmedrs1736020
geneviewrs1736020
scholarrs1736020
googlers1736020
pharmgkbrs1736020
gwascentralrs1736020
openSNPrs1736020
23andMers1736020
23andMe allrs1736020
SNP Nexus

SNPshotrs1736020
SNPdbers1736020
MSV3drs1736020
GWAS Ctlgrs1736020
GMAF0.2746
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 9E-12
Odds Ratio 1.16 [1.11-1.21]