MYH11, myosin heavy chain 11, 4629

N. diseases: 161; N. variants: 25
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3915499
rs3915499
Entrez Id: 4629
Gene Symbol: MYH11
MYH11
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019