MYL1, myosin light chain 1, 4632

N. diseases: 18; N. variants: 7
Disease: Serum albumin measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12469767
rs12469767
Entrez Id: 4632
Gene Symbol: MYL1
MYL1
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013