MYL2, myosin light chain 2, 4633

N. diseases: 104; N. variants: 28
Disease: Cardiomyopathies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1566147422
rs1566147422
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0878544
Disease:
Cardiomyopathies 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs751392310
rs751392310
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0878544
Disease:
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs104894369
rs104894369
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0878544
Disease:
Cardiomyopathies 		0.010 GeneticVariation BEFREE The co-segregation of the MYL2 R58Q mutation in Chinese hypertrophic cardiomyopathy family and its pathological effect on cardiomyopathy disarray. 31104103 2019
dbSNP: rs35049558
rs35049558
Entrez Id: 4633
Gene Symbol: MYL2
MYL2
CUI: C0878544
Disease:
Cardiomyopathies 		0.010 GeneticVariation BEFREE The co-segregation of the MYL2 R58Q mutation in Chinese hypertrophic cardiomyopathy family and its pathological effect on cardiomyopathy disarray. 31104103 2019