MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Disease: May-Hegglin anomaly ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797044804
rs797044804
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly 		A 0.700 CausalMutation CLINVAR