MYL3, myosin light chain 3, 4634

N. diseases: 37; N. variants: 17
Disease: Microalbuminuria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs73065147
rs73065147
Entrez Id: 4634
Gene Symbol: MYL3
MYL3
CUI: C0730345
Disease:
Microalbuminuria 		C 0.700 GeneticVariation GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532 2019