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rs359457

From SNPedia

Orientationplus
Stabilizedplus
Make rs359457(C;C)
Make rs359457(C;T)
Make rs359457(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position173852839
is asnp
is mentioned by
dbSNPrs359457
dbSNP (classic)rs359457
ClinGenrs359457
ebirs359457
HLIrs359457
Exacrs359457
Gnomadrs359457
Varsomers359457
LitVarrs359457
Maprs359457
PheGenIrs359457
Biobankrs359457
1000 genomesrs359457
hgdprs359457
ensemblrs359457
geneviewrs359457
scholarrs359457
googlers359457
pharmgkbrs359457
gwascentralrs359457
openSNPrs359457
23andMers359457
SNPshotrs359457
SNPdbers359457
MSV3drs359457
GWAS Ctlgrs359457
GMAF0.4692
Max Magnitude0
? (C;C) (C;T) (T;T) 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 T
P-val 3E-12
Odds Ratio 1.0800 [1.04-1.12]