Human SNP ID | rs1052501 |
---|---|
Human chromosome | chr3 |
Human SNP position | 41883906 |
Pig chromosome | chr13 |
Pig SNP position | 28294445 |
PubMed ID | 22120009 |
---|---|
Journal | Nat Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/22120009 |
Study | Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. |
Disease/Trait | Multiple myeloma |
Initial sample | 1,675 European ancestry cases, 5,903 European ancestry controls |
Replication sample | 169 European ancestry cases, 927 European ancestry controls |
Region | 3p22.1 |
Chromosome id | chr3 |
Chromosome position | 41883906 |
Reported gene | ULK4 |
Mapped gene | ULK4 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 54986 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1052501-G |
SNPs | rs1052501 |
Merged | 0 |
SNP id current | 1052501 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | 0.16 |
P value | 0.00000002 |
Pvalue mlog | 7.69897000433601 |
P value text | |
Or beta | 1.32 |
%95 Ci | [1.20-1.45] |
Platform | Illumina [422839] |
CNV | N |
Mapped trait | multiple myeloma |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0001378 |
Study accession | GCST001331 |