MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: Cataract ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338829
rs80338829
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0086543
Disease:
Cataract 		0.010 GeneticVariation BEFREE Two cases had Alport manifestations including deafness, nephritis, and cataracts and had R1165C and E1841K mutations, respectively. 11776386 2001