Human SNP ID | rs13401811 |
---|---|
Human chromosome | chr2 |
Human SNP position | 110858527 |
Pig chromosome | chr3 |
Pig SNP position | 47396076 |
PubMed ID | 23770605 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23770605 |
Study | Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. |
Disease/Trait | Chronic lymphocytic leukemia |
Initial sample | 2,179 European ancestry cases, 6,221 European ancestry controls |
Replication sample | 1,709 European ancestry cases, 6,318 European ancestry controls |
Region | 2q13 |
Chromosome id | chr2 |
Chromosome position | 110858527 |
Reported gene | ACOXL, BCL2L11 |
Mapped gene | ACOXL |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 55289 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs13401811-G |
SNPs | rs13401811 |
Merged | 0 |
SNP id current | 13401811 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.81 |
P value | 0.000000000000000002 |
Pvalue mlog | 17.698970004336 |
P value text | |
Or beta | 1.41 |
%95 Ci | [1.30-1.52] |
Platform | Illumina [549934] |
CNV | N |
Mapped trait | chronic lymphocytic leukemia |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000095 |
Study accession | GCST002073 |