Human SNP ID | rs2221433 |
---|---|
Human chromosome | chr16 |
Human SNP position | 10569770 |
Pig chromosome | chr3 |
Pig SNP position | 33260575 |
PubMed ID | 23568457 |
---|---|
Journal | Int J Eat Disord |
Link | www.ncbi.nlm.nih.gov/pubmed/23568457 |
Study | Genetic variants associated with disordered eating. |
Disease/Trait | Eating disorders |
Initial sample | 543 European ancestry female cases, 1,116 European ancestry female controls |
Replication sample | NA |
Region | 16p13.13 |
Chromosome id | chr16 |
Chromosome position | 10569770 |
Reported gene | TEKT5, EMP2 |
Mapped gene | EMP2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 2013 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2221433-G |
SNPs | rs2221433 |
Merged | 0 |
SNP id current | 2221433 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.682 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | 0.087 |
%95 Ci | [0.05-0.124] unit decrease |
Platform | Illumina [6150213] (imputed) |
CNV | N |
Mapped trait | eating disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005203 |
Study accession | GCST001960 |