Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
T | 0.800 | GeneticVariation | GWASCAT | The two strongest associations were SNP rs1354034 with MPV (p = 2.4x10-13) and rs855791 with MCV (p = 5.2x10-12). | 31194788 | 2019 |
|||
|
C | 0.800 | GeneticVariation | GWASCAT | The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. | 27863252 | 2016 |
|||
|
C | 0.800 | GeneticVariation | GWASCAT | A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. | 24026423 | 2014 |
|||
|
T | 0.800 | GeneticVariation | GWASCAT | New gene functions in megakaryopoiesis and platelet formation. | 22139419 | 2011 |
|||
|
A | 0.800 | GeneticVariation | GWASCAT | A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. | 19820697 | 2009 |
|||
|
A | 0.800 | GeneticVariation | GWASCAT | We conducted a genome-wide association study (GWAS), the KORA (Kooperative Gesundheitsforschung in der Region Augsburg) F3 500K study, and found MPV to be strongly associated with three common single-nucleotide polymorphisms (SNPs): rs7961894 located within intron 3 of WDR66 on chromosome 12q24.31, rs12485738 upstream of the ARHGEF3 on chromosome 3p13-p21, and rs2138852 located upstream of TAOK1 on chromosome 17q11.2. | 19110211 | 2009 |
|||
|
CA | 0.700 | GeneticVariation | GWASCAT | The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. | 27863252 | 2016 |
|||
|
T | 0.700 | GeneticVariation | GWASCAT | The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. | 27863252 | 2016 |
|||
|
A | 0.700 | GeneticVariation | GWASCAT | The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. | 27863252 | 2016 |