Human SNP ID | rs4362 |
---|---|
Human chromosome | chr17 |
Human SNP position | 63496400 |
Pig chromosome | chr12 |
Pig SNP position | 15382525 |
PubMed ID | 24816252 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/24816252 |
Study | An atlas of genetic influences on human blood metabolites. |
Disease/Trait | Blood metabolite levels |
Initial sample | 7,824 European ancestry individuals |
Replication sample | NA |
Region | 17q23.3 |
Chromosome id | chr17 |
Chromosome position | 63496400 |
Reported gene | ACE |
Mapped gene | ACE |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1636 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4362-T |
SNPs | rs4362 |
Merged | 0 |
SNP id current | 4362 |
Context | synonymous_variant |
Intergenic | 0 |
Allele frequency | 0.53 |
P value | 1E-21 |
Pvalue mlog | 21 |
P value text | (X-14208--phenylalanylserine) |
Or beta | 0.061 |
%95 Ci | [0.049-0.073] unit increase |
Platform | Affymetrix, Illumina [2100000] (imputed) |
CNV | N |
Mapped trait | blood metabolite measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005664 |
Study accession | GCST002443 |