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rs1728918

From SNPedia

Orientationplus
Stabilizedplus
Make rs1728918(A;A)
Make rs1728918(A;G)
Make rs1728918(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position27412596
is asnp
is mentioned by
dbSNPrs1728918
dbSNP (classic)rs1728918
ClinGenrs1728918
ebirs1728918
HLIrs1728918
Exacrs1728918
Gnomadrs1728918
Varsomers1728918
LitVarrs1728918
Maprs1728918
PheGenIrs1728918
Biobankrs1728918
1000 genomesrs1728918
hgdprs1728918
ensemblrs1728918
geneviewrs1728918
scholarrs1728918
googlers1728918
pharmgkbrs1728918
gwascentralrs1728918
openSNPrs1728918
23andMers1728918
SNPshotrs1728918
SNPdbers1728918
MSV3drs1728918
GWAS Ctlgrs1728918
GMAF0.2264
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Crohn's disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele A
P-val 5E-16
Odds Ratio 1.12 [1.086-1.16]