SNP Detail For rs13401811
1.Mapping Information
Human SNP ID rs13401811
Human chromosome chr2
Human SNP position 110858527
Pig chromosome chr3
Pig SNP position 47396076
2.Annotation Information
PubMed ID23770605
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23770605
StudyGenome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Disease/TraitChronic lymphocytic leukemia
Initial sample2,179 European ancestry cases, 6,221 European ancestry controls
Replication sample1,709 European ancestry cases, 6,318 European ancestry controls
Region2q13
Chromosome idchr2
Chromosome position110858527
Reported geneACOXL, BCL2L11
Mapped geneACOXL
Upstream gene id
Downstream gene id
SNP gene ids55289
Upstream gene distance
Downstream gene distance
SNP risk allelers13401811-G
SNPsrs13401811
Merged0
SNP id current13401811
Contextintron_variant
Intergenic0
Allele frequency0.81
P value0.000000000000000002
Pvalue mlog17.698970004336
P value text
Or beta1.41
%95 Ci[1.30-1.52]
PlatformIllumina [549934]
CNVN
Mapped traitchronic lymphocytic leukemia
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000095
Study accessionGCST002073