Human SNP ID | rs10757278 |
---|---|
Human chromosome | chr9 |
Human SNP position | 22124478 |
Pig chromosome | chr1 |
Pig SNP position | 223799098 |
PubMed ID | 17478679 |
---|---|
Journal | Science |
Link | www.ncbi.nlm.nih.gov/pubmed/17478679 |
Study | A common variant on chromosome 9p21 affects the risk of myocardial infarction. |
Disease/Trait | Myocardial infarction |
Initial sample | 1,607 European ancestry cases, 6,728 European ancestry controls |
Replication sample | 2,980 European ancestry cases, 6,309 European ancestry controls |
Region | 9p21.3 |
Chromosome id | chr9 |
Chromosome position | 22124478 |
Reported gene | CDKN2A, CDKN2B |
Mapped gene | CDKN2B-AS1 - DMRTA1 |
Upstream gene id | 100048912 |
Downstream gene id | 63951 |
SNP gene ids | |
Upstream gene distance | 3381 |
Downstream gene distance | 322363 |
SNP risk allele | rs10757278-G |
SNPs | rs10757278 |
Merged | 0 |
SNP id current | 10757278 |
Context | downstream_gene_variant |
Intergenic | 1 |
Allele frequency | 0.45 |
P value | 1E-20 |
Pvalue mlog | 20 |
P value text | |
Or beta | 1.28 |
%95 Ci | [1.22-1.35] |
Platform | Illumina [305953] |
CNV | N |
Mapped trait | myocardial infarction |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000612 |
Study accession | GCST000030 |