Human SNP ID | rs944797 |
---|---|
Human chromosome | chr9 |
Human SNP position | 22115287 |
Pig chromosome | chr1 |
Pig SNP position | 223805953 |
PubMed ID | 21971053 |
---|---|
Journal | Eur J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21971053 |
Study | Genome-wide association study of coronary artery disease in the Japanese. |
Disease/Trait | Coronary heart disease |
Initial sample | 806 Japanese ancestry cases, 1,337 Japanese ancestry controls |
Replication sample | 3,593 Japanese ancestry cases, 6,335 Japanese ancestry controls |
Region | 9p21.3 |
Chromosome id | chr9 |
Chromosome position | 22115287 |
Reported gene | CDKN2A, CDKN2B |
Mapped gene | CDKN2B-AS1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 100048912 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs944797-C |
SNPs | rs944797 |
Merged | 0 |
SNP id current | 944797 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.46 |
P value | 0.0000000000000006 |
Pvalue mlog | 15.2218487496163 |
P value text | |
Or beta | 1.25 |
%95 Ci | [1.18-1.31] |
Platform | Illumina [451382] |
CNV | N |
Mapped trait | coronary heart disease |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001645 |
Study accession | GCST001260 |