MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: Kidney Failure, Chronic ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3752462
rs3752462
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0022661
Disease:
Kidney Failure, Chronic 		0.010 GeneticVariation BEFREE MYH9 SNPs rs4821480, rs2032487, rs4281481 and rs3752462 are associated with T2DM-ESRD susceptibility in European Americans. 21968013 2012