Human SNP ID | rs4737547 |
---|---|
Human chromosome | chr8 |
Human SNP position | 59633105 |
Pig chromosome | chr4 |
Pig SNP position | 80135277 |
PubMed ID | 23502783 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/23502783 |
Study | The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. |
Disease/Trait | Multiple myeloma (IgH translocation) |
Initial sample | up to 1,660 European ancestry cases, 7,306 European ancestry controls |
Replication sample | |
Region | 8q12.1 |
Chromosome id | chr8 |
Chromosome position | 59633105 |
Reported gene | NR |
Mapped gene | LOC105375859 - LOC105375862 |
Upstream gene id | 105375859 |
Downstream gene id | 105375862 |
SNP gene ids | |
Upstream gene distance | 12907 |
Downstream gene distance | 413678 |
SNP risk allele | rs4737547-G |
SNPs | rs4737547 |
Merged | 0 |
SNP id current | 4737547 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.42 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | (Any IgH translocation vs. controls) |
Or beta | 1.3 |
%95 Ci | [1.17-1.45] |
Platform | Illumina [414804] (imputed) |
CNV | N |
Mapped trait | multiple myeloma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001378 |
Study accession | GCST001906 |