WDR66, WD repeat domain 66, 144406

N. diseases: 26; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASCAT GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort. 31194788 2019
Red cell distribution width determination
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
RDW - Red blood cell distribution width result
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0021704
Disease: Intelligence
Intelligence
0.100 GeneticVariation phenotype GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
CUI: C1305855
Disease: Body mass index
Body mass index
0.100 GeneticVariation phenotype GWASCAT Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. 29273807 2018
CUI: C4082176
Disease: Asthenozoospermia finding
Asthenozoospermia finding
0.100 CausalMutation phenotype CLINVAR Loss of Calmodulin- and Radial-Spoke-Associated Complex Protein CFAP251 Leads to Immotile Spermatozoa Lacking Mitochondria and Infertility in Men. 30122541 2018
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASDB A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. 24026423 2014
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASCAT A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. 24026423 2014
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASDB A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. 22423221 2012
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.100 GeneticVariation phenotype GWASCAT New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.100 GeneticVariation phenotype GWASDB New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASDB New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASCAT New gene functions in megakaryopoiesis and platelet formation. 22139419 2011
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASDB A genome-wide association study identifies three loci associated with mean platelet volume. 19110211 2009
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASDB A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. 19820697 2009
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASCAT A genome-wide association study identifies three loci associated with mean platelet volume. 19110211 2009
Platelet mean volume determination (procedure)
0.100 GeneticVariation phenotype GWASCAT A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. 19820697 2009
CUI: C0021359
Disease: Infertility
Infertility
0.100 Biomarker phenotype HPO
CUI: C4022699
Disease: Sperm tail anomaly
Sperm tail anomaly
0.100 CausalMutation phenotype CLINVAR
CUI: C4022700
Disease: Sperm mid-piece anomaly
Sperm mid-piece anomaly
0.100 CausalMutation phenotype CLINVAR
CUI: C4539786
Disease: Absent sperm flagella
Absent sperm flagella
0.100 Biomarker phenotype HPO
CUI: C4539787
Disease: Short sperm flagella
Short sperm flagella
0.100 Biomarker phenotype HPO
CUI: C4539789
Disease: Coiled sperm flagella
Coiled sperm flagella
0.100 Biomarker phenotype HPO