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rs273900

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;T) 0 common in complete genomics
Make rs273900(C;C)
Make rs273900(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132358913
GeneLOC553103
is asnp
is mentioned by
dbSNPrs273900
ebirs273900
HLIrs273900
Exacrs273900
Varsomers273900
Maprs273900
PheGenIrs273900
hapmaprs273900
1000 genomesrs273900
hgdprs273900
ensemblrs273900
gopubmedrs273900
geneviewrs273900
scholarrs273900
googlers273900
pharmgkbrs273900
gwascentralrs273900
openSNPrs273900
23andMers273900
23andMe allrs273900
SNP Nexus

SNPshotrs273900
SNPdbers273900
MSV3drs273900
GWAS Ctlgrs273900
GMAF0.4417
Max Magnitude0
[PMID 18668679] rs272893 and rs273900 are associated with Crohn's disease (OR 2.16; 95% CI 1.21-3.59 and OR 2.40; 95% CI 1.43-4.05)


[PMID 17476680] Genetic susceptibility has a more important role in pediatric-onset Crohn's disease than in adult-onset Crohn's disease.