Human SNP ID | rs11655237 |
---|---|
Human chromosome | chr17 |
Human SNP position | 72404025 |
Pig chromosome | chr12 |
Pig SNP position | 8820133 |
PubMed ID | 26098869 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/26098869 |
Study | Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. |
Disease/Trait | Pancreatic cancer |
Initial sample | 7,638 cases, 7,364 controls |
Replication sample | 2,287 cases, 4,205 controls |
Region | 17q24.3 |
Chromosome id | chr17 |
Chromosome position | 72404025 |
Reported gene | LINC00673 |
Mapped gene | LINC00673 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 100499467 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11655237-T |
SNPs | rs11655237 |
Merged | |
SNP id current | 11655237 |
Context | non_coding_transcript_exon_variant |
Intergenic | 0 |
Allele frequency | 0.11 |
P value | 0.00000000000001 |
Pvalue mlog | 14 |
P value text | |
Or beta | 1.26 |
%95 Ci | [1.19-1.34] |
Platform | Illumina [866891] (imputed) |
CNV | N |
Mapped trait | pancreatic carcinoma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0002618 |
Study accession | GCST002991 |