Human SNP ID | rs1337875 |
---|---|
Human chromosome | chr1 |
Human SNP position | 247895248 |
Pig chromosome | chr2 |
Pig SNP position | 56439808 |
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 | 1q44 |
Chromosome id | chr1 |
Chromosome position | 247895248 |
Reported gene | NR |
Mapped gene | TRIM58 - OR2W3 |
Upstream gene id | 25893 |
Downstream gene id | 343171 |
SNP gene ids | |
Upstream gene distance | 15110 |
Downstream gene distance | 339 |
SNP risk allele | rs1337875-G |
SNPs | rs1337875 |
Merged | |
SNP id current | 1337875 |
Context | upstream_gene_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | |
Or beta | 1.37 |
%95 Ci | [NR] |
Platform | Illumina [720770] |
CNV | N |
Mapped trait | Pituitary Gland Adenoma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_1000478 |
Study accession | GCST002940 |