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rs6651252

From SNPedia

Orientationplus
Stabilizedplus
Make rs6651252(C;C)
Make rs6651252(C;T)
Make rs6651252(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position128554935
GeneLINC00824
is asnp
is mentioned by
dbSNPrs6651252
ebirs6651252
HLIrs6651252
Exacrs6651252
Varsomers6651252
Maprs6651252
PheGenIrs6651252
hapmaprs6651252
1000 genomesrs6651252
hgdprs6651252
ensemblrs6651252
gopubmedrs6651252
geneviewrs6651252
scholarrs6651252
googlers6651252
pharmgkbrs6651252
gwascentralrs6651252
openSNPrs6651252
23andMers6651252
23andMe allrs6651252
SNP Nexus

SNPshotrs6651252
SNPdbers6651252
MSV3drs6651252
GWAS Ctlgrs6651252
GMAF0.1423
Max Magnitude
? (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 4E-18
Odds Ratio 1.2300 [1.17-1.30]
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 T
P-val 1E-16
Odds Ratio 1.19 [1.128-1.246]