Human SNP ID | rs6686929 |
---|---|
Human chromosome | chr1 |
Human SNP position | 17918213 |
Pig chromosome | chr6 |
Pig SNP position | 70795036 |
PubMed ID | 23251661 |
---|---|
Journal | PLoS One |
Link | www.ncbi.nlm.nih.gov/pubmed/23251661 |
Study | Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. |
Disease/Trait | Obesity-related traits |
Initial sample | 815 Hispanic children from 263 families |
Replication sample | NA |
Region | 1p36.13 |
Chromosome id | chr1 |
Chromosome position | 17918213 |
Reported gene | ACTL8 |
Mapped gene | ACTL8 - LOC105376809 |
Upstream gene id | 81569 |
Downstream gene id | 105376809 |
SNP gene ids | |
Upstream gene distance | 91150 |
Downstream gene distance | 82209 |
SNP risk allele | rs6686929-G |
SNPs | rs6686929 |
Merged | 0 |
SNP id current | 6686929 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.486 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | (Ghrelin ) |
Or beta | 0.03 |
%95 Ci | [NR] pg/100 碌L increase |
Platform | Illumina [899892] |
CNV | N |
Mapped trait | hormone measurement |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004730 |
Study accession | GCST001762 |