SNP Detail For rs11064881
1.Mapping Information
Human SNP ID rs11064881
Human chromosome chr12
Human SNP position 119709120
Pig chromosome chr14
Pig SNP position 35126972
2.Annotation Information
PubMed ID26192919
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/26192919
StudyAssociation analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
Disease/TraitUlcerative colitis
Initial sample6,968 European ancestry cases, 20,464 European ancestry controls
Replication sample10,679 European ancestry cases, 26,715 European ancestry controls, 397 Iranian ancestry cases, 342 Iranian ancestry controls, 1,239 Indian ancestry cases, 990 Indian ancestry controls, 1,134 East Asian ancestry cases, 3,719 East Asian ancestry controls
Region12q24.23
Chromosome idchr12
Chromosome position119709120
Reported genePRKAB1
Mapped geneCIT
Upstream gene id
Downstream gene id
SNP gene ids11113
Upstream gene distance
Downstream gene distance
SNP risk allelers11064881-A
SNPsrs11064881
Merged
SNP id current11064881
Contextintron_variant
Intergenic0
Allele frequency0.07342
P value0.0000002
Pvalue mlog6.69897000433601
P value text(EA)
Or beta1.1273501
%95 Ci[1.08-1.17]
PlatformAffymetrix, Illumina [~ 9000000] (imputed)
CNVN
Mapped traitulcerative colitis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000729
Study accessionGCST003045
PubMed ID26192919
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/26192919
StudyAssociation analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
Disease/TraitInflammatory bowel disease
Initial sample12,882 European ancestry cases, 21,770 European ancestry controls
Replication sample25,273 European ancestry cases, 26,715 European ancestry controls, 548 Iranian ancestry cases, 342 Iranian ancestry control, 1,423 Indian ancestry cases, 990 Indian ancestry controls, 2,824 East Asian ancestry cases, 3,719 East Asian ancestry controls
Region12q24.23
Chromosome idchr12
Chromosome position119709120
Reported genePRKAB1
Mapped geneCIT
Upstream gene id
Downstream gene id
SNP gene ids11113
Upstream gene distance
Downstream gene distance
SNP risk allelers11064881-A
SNPsrs11064881
Merged
SNP id current11064881
Contextintron_variant
Intergenic0
Allele frequency0.07342
P value0.00000006
Pvalue mlog7.22184874961635
P value text(EA)
Or beta1.1044849
%95 Ci[1.07-1.14]
PlatformAffymetrix, Illumina [~ 9000000] (imputed)
CNVN
Mapped traitinflammatory bowel disease
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003767
Study accessionGCST003043