MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: Anemia, Sickle Cell ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.020 GeneticVariation disease BEFREE In sickle cell disease (SCD) patients, we reported previously a genetic interaction between APOL1 and MYH9. 26147622 2015
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		0.020 GeneticVariation disease BEFREE We genotyped 26 single nucleotide polymorphisms (SNPs) in MYH9 and 2 SNPs in APOL1 (representing the G1 and G2 tags) in 521 unrelated adult (18-83 years) SCD patients screened for proteinuria. 21910715 2011