Human SNP ID | rs6959888 |
---|---|
Human chromosome | chr7 |
Human SNP position | 88967071 |
Pig chromosome | chr9 |
Pig SNP position | 75582041 |
PubMed ID | 21079607 |
---|---|
Journal | Mol Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/21079607 |
Study | A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. |
Disease/Trait | Anorexia nervosa |
Initial sample | 1,033 European ancestry cases, 3,733 European ancestry controls |
Replication sample | NA |
Region | 7q21.13 |
Chromosome id | chr7 |
Chromosome position | 88967071 |
Reported gene | ZNF804B |
Mapped gene | ZNF804B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 219578 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs6959888-? |
SNPs | rs6959888 |
Merged | 0 |
SNP id current | 6959888 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.11 |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [~ 598000] |
CNV | N |
Mapped trait | anorexia nervosa |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004215 |
Study accession | GCST000873 |