MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13053731
rs13053731
Entrez Id: 4627;102465491
Gene Symbol: MYH9;MIR6819
MYH9;MIR6819
CUI: C1285654
Disease:
Memory performance
0.700 GeneticVariation GWASCAT Genome-wide association study of language performance in Alzheimer's disease. 28577822 2017