Human SNP ID | rs12034383 |
---|---|
Human chromosome | chr1 |
Human SNP position | 207630250 |
Pig chromosome | chr9 |
Pig SNP position | 74562097 |
PubMed ID | 21700265 |
---|---|
Journal | Am J Hum Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/21700265 |
Study | Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. |
Disease/Trait | Erythrocyte sedimentation rate |
Initial sample | 1,979 European ancestry individuals |
Replication sample | 5,628 European ancestry individuals |
Region | 1q32.2 |
Chromosome id | chr1 |
Chromosome position | 207630250 |
Reported gene | CR1 |
Mapped gene | CR1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1378 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs12034383-G |
SNPs | rs12034383 |
Merged | 0 |
SNP id current | 12034383 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.41 |
P value | 2E-28 |
Pvalue mlog | 27.698970004336 |
P value text | |
Or beta | 0.13 |
%95 Ci | [NR] unit decrease |
Platform | Illumina [476395] |
CNV | N |
Mapped trait | blood sedimentation |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004304 |
Study accession | GCST001120 |