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rs1551398

From SNPedia

Orientationminus
Stabilizedminus
Make rs1551398(C;C)
Make rs1551398(C;T)
Make rs1551398(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position125527809
GeneLOC105375746
is asnp
is mentioned by
dbSNPrs1551398
dbSNP (classic)rs1551398
ClinGenrs1551398
ebirs1551398
HLIrs1551398
Exacrs1551398
Gnomadrs1551398
Varsomers1551398
LitVarrs1551398
Maprs1551398
PheGenIrs1551398
Biobankrs1551398
1000 genomesrs1551398
hgdprs1551398
ensemblrs1551398
geneviewrs1551398
scholarrs1551398
googlers1551398
pharmgkbrs1551398
gwascentralrs1551398
openSNPrs1551398
23andMers1551398
SNPshotrs1551398
SNPdbers1551398
MSV3drs1551398
GWAS Ctlgrs1551398
GMAF0.4311
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 18587394OA-icon.png]
Trait Crohn's disease
Title Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease
Risk Allele A
P-val 5.0000000000000001E-9
Odds Ratio 1.08 [NR]

DeCode reports that rs1551398 is associated with susceptibility to Crohn's disease. [PMID 18587394OA-icon.png]


[PMID 19068216OA-icon.png] Investigation of Crohn's disease risk loci in ulcerative colitis further defines their molecular relationship.


[PMID 21304977OA-icon.png] An investigation of genome-wide studies reported susceptibility loci for ulcerative colitis shows limited replication in north Indians.



[PMID 23543094OA-icon.png] Testing for associations between loci and environmental gradients using latent factor mixed models.