Human SNP ID | rs1556640 |
---|---|
Human chromosome | chr6 |
Human SNP position | 138104895 |
Pig chromosome | JH118751-1 |
Pig SNP position | 10227 |
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 | Bulimia nervosa |
Initial sample | 151 European ancestry female cases, 2,291 European ancestry female controls |
Replication sample | NA |
Region | 6q23.3 |
Chromosome id | chr6 |
Chromosome position | 138104895 |
Reported gene | PERP |
Mapped gene | PERP |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 64065 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1556640-T |
SNPs | rs1556640 |
Merged | 0 |
SNP id current | 1556640 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.88 |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | 0.075 |
%95 Ci | [0.044-0.106] unit decrease |
Platform | Illumina [6150213] (imputed) |
CNV | N |
Mapped trait | bulimia nervosa |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005204 |
Study accession | GCST001958 |