Human SNP ID | rs61742849 |
---|---|
Human chromosome | chr1 |
Human SNP position | 113683521 |
Pig chromosome | chr4 |
Pig SNP position | 117029660 |
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 | 1p13.2 |
Chromosome id | chr1 |
Chromosome position | 113683521 |
Reported gene | PHTF1, MAGI3 |
Mapped gene | MAGI3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 260425 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs61742849-G |
SNPs | rs61742849 |
Merged | 0 |
SNP id current | 61742849 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.975 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | |
Or beta | 0.179 |
%95 Ci | [0.1-0.26] 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 |