Human SNP ID | rs4713169 |
---|---|
Human chromosome | chr6 |
Human SNP position | 11084321 |
Pig chromosome | chr7 |
Pig SNP position | 8184440 |
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 | 6p24.2 |
Chromosome id | chr6 |
Chromosome position | 11084321 |
Reported gene | ELOVL2 |
Mapped gene | ELOVL2-AS1 - SMIM13 |
Upstream gene id | 100506409 |
Downstream gene id | 221710 |
SNP gene ids | |
Upstream gene distance | 5177 |
Downstream gene distance | 9712 |
SNP risk allele | rs4713169-C |
SNPs | rs4713169 |
Merged | 0 |
SNP id current | 4713169 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.42 |
P value | 0.00000000000003 |
Pvalue mlog | 13.5228787452803 |
P value text | (X-12627) |
Or beta | 0.032 |
%95 Ci | [0.024-0.040] unit decrease |
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 |