Human SNP ID | rs17083838 |
---|---|
Human chromosome | chr13 |
Human SNP position | 26336975 |
Pig chromosome | chr11 |
Pig SNP position | 3529635 |
PubMed ID | 26029870 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/26029870 |
Study | Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma. |
Disease/Trait | Sporadic pituitary adenoma |
Initial sample | 771 Han Chinese cases, 2,788 Han Chinese controls |
Replication sample | 2,542 Han Chinese cases, 3,620 Han Chinese controls |
Region | 13q12.13 |
Chromosome id | chr13 |
Chromosome position | 26336975 |
Reported gene | CDK8, RNF6, WASF3 |
Mapped gene | CDK8 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1024 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs17083838-A |
SNPs | rs17083838 |
Merged | |
SNP id current | 17083838 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.104 |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | 1.37 |
%95 Ci | [1.23-1.53] |
Platform | Illumina [720770] |
CNV | N |
Mapped trait | Pituitary Gland Adenoma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_1000478 |
Study accession | GCST002940 |