Human SNP ID | rs6726292 |
---|---|
Human chromosome | chr2 |
Human SNP position | 54929493 |
Pig chromosome | chr3 |
Pig SNP position | 91091937 |
PubMed ID | 19553259 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19553259 |
Study | Common body mass index-associated variants confer risk of extreme obesity. |
Disease/Trait | Obesity (extreme) |
Initial sample | 775 European ancestry cases, 3,197 European ancestry controls |
Replication sample | NA |
Region | 2p16.1 |
Chromosome id | chr2 |
Chromosome position | 54929493 |
Reported gene | RTN4 |
Mapped gene | EML6 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 400954 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6726292-G |
SNPs | rs6726292 |
Merged | 0 |
SNP id current | 6726292 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.73 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 1.39 |
%95 Ci | [1.22-1.59] |
Platform | Illumina [457251] |
CNV | N |
Mapped trait | obesity |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001073 |
Study accession | GCST000426 |