Human SNP ID | rs4073582 |
---|---|
Human chromosome | chr11 |
Human SNP position | 66283241 |
Pig chromosome | chr2 |
Pig SNP position | 5179619 |
PubMed ID | 25646370 |
---|---|
Journal | Ann Rheum Dis |
Link | www.ncbi.nlm.nih.gov/pubmed/25646370 |
Study | Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes. |
Disease/Trait | Gout |
Initial sample | 945 Japanese ancestry cases, 1,213 Japanese ancestry controls |
Replication sample | 1,048 Japanese ancestry cases, 1,334 Japanese ancestry controls |
Region | 11q13.2 |
Chromosome id | chr11 |
Chromosome position | 66283241 |
Reported gene | CNIH-2 |
Mapped gene | CNIH2 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 254263 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4073582-G |
SNPs | rs4073582 |
Merged | 0 |
SNP id current | 4073582 |
Context | splice_region_variant |
Intergenic | 0 |
Allele frequency | 0.91 |
P value | 0.000000006 |
Pvalue mlog | 8.22184874961635 |
P value text | |
Or beta | 1.66 |
%95 Ci | [1.40-1.96] |
Platform | Illumina [570442] |
CNV | N |
Mapped trait | gout |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004274 |
Study accession | GCST002773 |