Human SNP ID | rs10180663 |
---|---|
Human chromosome | chr2 |
Human SNP position | 25410373 |
Pig chromosome | chr3 |
Pig SNP position | 120430167 |
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 | 2p23.3 |
Chromosome id | chr2 |
Chromosome position | 25410373 |
Reported gene | NR |
Mapped gene | DTNB |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1838 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs10180663-A |
SNPs | rs10180663 |
Merged | 0 |
SNP id current | 10180663 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.69 |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
P value text | (t11;14 vs. controls) |
Or beta | 1.64 |
%95 Ci | [1.34-2.02] |
Platform | Illumina [414804] (imputed) |
CNV | N |
Mapped trait | multiple myeloma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001378 |
Study accession | GCST001906 |