Human SNP ID | rs7090445 |
---|---|
Human chromosome | chr10 |
Human SNP position | 61961417 |
Pig chromosome | chr14 |
Pig SNP position | 70467763 |
PubMed ID | 23996088 |
---|---|
Journal | Blood |
Link | www.ncbi.nlm.nih.gov/pubmed/23996088 |
Study | Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. |
Disease/Trait | Acute lymphoblastic leukemia (B-cell precursor) |
Initial sample | 1,658 European ancestry child cases, 4,723 European ancestry controls |
Replication sample | 1,449 European ancestry child cases, 1,488 European ancestry controls |
Region | 10q21.2 |
Chromosome id | chr10 |
Chromosome position | 61961417 |
Reported gene | ARID5B |
Mapped gene | ARID5B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 84159 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7090445-? |
SNPs | rs7090445 |
Merged | 0 |
SNP id current | 7090445 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 5E-54 |
Pvalue mlog | 53.3010299956639 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [382776] (imputed) |
CNV | N |
Mapped trait | B-cell acute lymphoblastic leukemia |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000094 |
Study accession | GCST002158 |