Human SNP ID | rs2390582 |
---|---|
Human chromosome | chr1 |
Human SNP position | 90478350 |
Pig chromosome | chr4 |
Pig SNP position | 138126722 |
PubMed ID | 17903303 |
---|---|
Journal | BMC Med Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/17903303 |
Study | Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI__s Framingham Heart Study. |
Disease/Trait | Coronary artery calcification |
Initial sample | Up to 678 individuals |
Replication sample | NA |
Region | 1p22.2 |
Chromosome id | chr1 |
Chromosome position | 90478350 |
Reported gene | intergenic |
Mapped gene | LOC105378851 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105378851 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2390582-? |
SNPs | rs2390582 |
Merged | 0 |
SNP id current | 2390582 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Affymetrix [70897] |
CNV | N |
Mapped trait | coronary artery calcification |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004723 |
Study accession | GCST000097 |