Human SNP ID | rs138206701 |
---|---|
Human chromosome | chr5 |
Human SNP position | 81110747 |
Pig chromosome | chr2 |
Pig SNP position | 91588825 |
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 (purging via substances) |
Initial sample | 600 European ancestry female cases, 1,921 European ancestry female controls |
Replication sample | NA |
Region | 5q14.1 |
Chromosome id | chr5 |
Chromosome position | 81110747 |
Reported gene | RASGRF2 |
Mapped gene | RASGRF2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 5924 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs138206701-A |
SNPs | rs138206701 |
Merged | 0 |
SNP id current | 138206701 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.98 |
P value | 0.0000001 |
Pvalue mlog | 7 |
P value text | |
Or beta | 0.327 |
%95 Ci | [0.21-0.45] 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 | GCST001959 |
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 | 5q14.1 |
Chromosome id | chr5 |
Chromosome position | 81110747 |
Reported gene | RASGRF2 |
Mapped gene | RASGRF2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 5924 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs138206701-A |
SNPs | rs138206701 |
Merged | 0 |
SNP id current | 138206701 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.98 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | 0.425 |
%95 Ci | [0.24-0.61] 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 |