MYL1, myosin light chain 1, 4632

N. diseases: 18; N. variants: 7
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
dbSNP: rs1995836
rs1995836
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
dbSNP: rs2063311
rs2063311
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
dbSNP: rs2136457
rs2136457
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
dbSNP: rs6725084
rs6725084
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
dbSNP: rs6735154
rs6735154
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
dbSNP: rs6736750
rs6736750
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