Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2040571
rs2040571
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0200633
Disease:
Neutrophil count (procedure)
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018