Human SNP ID | rs1557305 |
---|---|
Human chromosome | chr18 |
Human SNP position | 4721359 |
Pig chromosome | chr6 |
Pig SNP position | 95243866 |
PubMed ID | 22911880 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/22911880 |
Study | Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits. |
Disease/Trait | Eating disorders |
Initial sample | Up to 2,567 European ancestry individuals |
Replication sample | Up to 767 European ancestry cases, up to 486 European ancestry controls |
Region | 18p11.31 |
Chromosome id | chr18 |
Chromosome position | 4721359 |
Reported gene | DLGAP1 |
Mapped gene | LOC105371968 - PPIAP14 |
Upstream gene id | 105371968 |
Downstream gene id | 5486 |
SNP gene ids | |
Upstream gene distance | 224966 |
Downstream gene distance | 281193 |
SNP risk allele | rs1557305-C |
SNPs | rs1557305 |
Merged | 0 |
SNP id current | 1557305 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.628 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | (OCPD) |
Or beta | 1.11 |
%95 Ci | [1.06-1.16] |
Platform | Illumina [283744] |
CNV | N |
Mapped trait | mental or behavioural disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0000677 |
Study accession | GCST001644 |