Human SNP ID | rs10492681 |
---|---|
Human chromosome | chr13 |
Human SNP position | 40233346 |
Pig chromosome | JH118429-1 |
Pig SNP position | 10711 |
PubMed ID | 17903293 |
---|---|
Journal | BMC Med Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/17903293 |
Study | Genome-wide association with select biomarker traits in the Framingham Heart Study. |
Disease/Trait | Select biomarker traits |
Initial sample | 1,012 European ancestry individuals |
Replication sample | NA |
Region | 13q14.11 |
Chromosome id | chr13 |
Chromosome position | 40233346 |
Reported gene | intergenic |
Mapped gene | LOC105370172 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105370172 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10492681-? |
SNPs | rs10492681 |
Merged | 0 |
SNP id current | 10492681 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (ALT) |
Or beta | |
%95 Ci | |
Platform | Affymetrix [70897] |
CNV | N |
Mapped trait | serum alanine aminotransferase measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004735 |
Study accession | GCST000083 |