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rs559928

From SNPedia

Orientationplus
Stabilizedplus
Make rs559928(C;C)
Make rs559928(C;T)
Make rs559928(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64382898
is asnp
is mentioned by
dbSNPrs559928
dbSNP (classic)rs559928
ClinGenrs559928
ebirs559928
HLIrs559928
Exacrs559928
Gnomadrs559928
Varsomers559928
LitVarrs559928
Maprs559928
PheGenIrs559928
Biobankrs559928
1000 genomesrs559928
hgdprs559928
ensemblrs559928
geneviewrs559928
scholarrs559928
googlers559928
pharmgkbrs559928
gwascentralrs559928
openSNPrs559928
23andMers559928
SNPshotrs559928
SNPdbers559928
MSV3drs559928
GWAS Ctlgrs559928
GMAF0.1864
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Inflammatory bowel disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele C
P-val 4E-11
Odds Ratio 1.10 [1.061-1.142]