Human SNP ID | rs1898111 |
---|---|
Human chromosome | chr15 |
Human SNP position | 47600101 |
Pig chromosome | chr1 |
Pig SNP position | 138233645 |
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 | 15q21.1 |
Chromosome id | chr15 |
Chromosome position | 47600101 |
Reported gene | SEMA6D |
Mapped gene | LOC105370804, SEMA6D |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105370804, 80031 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1898111-A |
SNPs | rs1898111 |
Merged | 0 |
SNP id current | 1898111 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.837 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (OCPD) |
Or beta | 1.15 |
%95 Ci | [1.08-1.22] |
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 |