Human SNP ID | rs2926702 |
---|---|
Human chromosome | chr8 |
Human SNP position | 70255759 |
Pig chromosome | chr4 |
Pig SNP position | 70793584 |
PubMed ID | 23144319 |
---|---|
Journal | Carcinogenesis |
Link | www.ncbi.nlm.nih.gov/pubmed/23144319 |
Study | Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study. |
Disease/Trait | Non-small cell lung cancer |
Initial sample | 348 Korean ancestry cases |
Replication sample | NA |
Region | 8q13.3 |
Chromosome id | chr8 |
Chromosome position | 70255759 |
Reported gene | NCOA2 |
Mapped gene | NCOA2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 10499 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2926702-T |
SNPs | rs2926702 |
Merged | 0 |
SNP id current | 2926702 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.572 |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | (Additive model) |
Or beta | |
%95 Ci | |
Platform | Affymetrix [271817] |
CNV | N |
Mapped trait | non-small cell lung carcinoma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003060 |
Study accession | GCST001734 |