Human SNP ID | rs56156506 |
---|---|
Human chromosome | chrX |
Human SNP position | 38140399 |
Pig chromosome | chrX |
Pig SNP position | 37870124 |
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 | Anorexia nervosa |
Initial sample | 237 European ancestry female cases, 2,287 European ancestry female controls |
Replication sample | NA |
Region | Xp11.4 |
Chromosome id | chrX |
Chromosome position | 38140399 |
Reported gene | SYTL5 |
Mapped gene | SYTL5 - SRPX |
Upstream gene id | 94122 |
Downstream gene id | 8406 |
SNP gene ids | |
Upstream gene distance | 11105 |
Downstream gene distance | 8936 |
SNP risk allele | rs56156506-A |
SNPs | rs56156506 |
Merged | 0 |
SNP id current | 56156506 |
Context | intron_variant |
Intergenic | 1 |
Allele frequency | 0.813 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 0.053 |
%95 Ci | [0.031-0.075] unit decrease |
Platform | Illumina [6150213] (imputed) |
CNV | N |
Mapped trait | anorexia nervosa |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004215 |
Study accession | GCST001961 |