MYO6, myosin VI, 4646

N. diseases: 66; N. variants: 22
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: rs2295938
rs2295938
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs2312933
rs2312933
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs6453843
rs6453843
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs9294004
rs9294004
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
dbSNP: rs9359145
rs9359145
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0523465
Disease:
Serum albumin measurement 		0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013