MYO6, myosin VI, 4646

N. diseases: 66; N. variants: 22
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1280049
rs1280049
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs9443189
rs9443189
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0600139
Disease:
Prostate carcinoma 		G 0.700 GeneticVariation GWASCAT A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer. 25217961 2014
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
dbSNP: rs3798440
rs3798440
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0020538
Disease:
Hypertensive disease 		0.700 GeneticVariation GWASDB Two-marker association tests yield new disease associations for coronary artery disease and hypertension. 21626137 2011
dbSNP: rs9350602
rs9350602
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0020538
Disease:
Hypertensive disease 		0.700 GeneticVariation GWASDB Two-marker association tests yield new disease associations for coronary artery disease and hypertension. 21626137 2011
dbSNP: rs121912560
rs121912560
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		0.700 GeneticVariation UNIPROT Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6). 15060111 2004
dbSNP: rs121912559
rs121912559
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C1843028
Disease:
Deafness, Autosomal Recessive 37 		0.700 GeneticVariation UNIPROT Mutations of MYO6 are associated with recessive deafness, DFNB37. 12687499 2003
dbSNP: rs1060499799
rs1060499799
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121912557
rs121912557
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121912558
rs121912558
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C1843028
Disease:
Deafness, Autosomal Recessive 37 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121912560
rs121912560
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C3501265
Disease:
Deafness, Sensorineural, with Hypertrophic Cardiomyopathy 		G 0.700 CausalMutation CLINVAR
dbSNP: rs121912561
rs121912561
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1554218566
rs1554218566
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C1843156
Disease:
Progressive sensorineural hearing impairment 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1554218566
rs1554218566
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1562201376
rs1562201376
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C1843028
Disease:
Deafness, Autosomal Recessive 37 		CT 0.700 CausalMutation CLINVAR
dbSNP: rs1562283089
rs1562283089
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		G 0.700 CausalMutation CLINVAR
dbSNP: rs727503326
rs727503326
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		T 0.700 CausalMutation CLINVAR
dbSNP: rs727503326
rs727503326
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C1843028
Disease:
Deafness, Autosomal Recessive 37 		T 0.700 CausalMutation CLINVAR
dbSNP: rs727504567
rs727504567
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		T 0.700 CausalMutation CLINVAR
dbSNP: rs878853225
rs878853225
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C2931767
Disease:
Deafness, autosomal dominant nonsyndromic sensorineural 22 		C 0.700 CausalMutation CLINVAR
dbSNP: rs121912557
rs121912557
Entrez Id: 4646
Gene Symbol: MYO6
MYO6
CUI: C0018784
Disease:
Sensorineural Hearing Loss (disorder) 		0.020 GeneticVariation BEFREE Heterozygous Myo6-C442Y mice recapitulated the progressive postlingual sensorineural deafness in human, thus providing a useful model for elucidating the role myosin VI plays in the mammalian auditory system. 31103816 2019