DisGeNET - a database of gene-disease associations

Cardiomyopathies, C0878544

Gene: MYL3 ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	4634
Gene Symbol:	MYL3

MYL3

0.410

GeneticVariation

group

BEFREE

MYL2 and MYL3 mutations are rare and the least cause of cardiomyopathies in Indians.

2018

Entrez Id:	4634
Gene Symbol:	MYL3

MYL3

0.410

Biomarker

group

GENOMICS_ENGLAND

Entrez Id:	4634
Gene Symbol:	MYL3

MYL3

0.410

GeneticVariation

group

CLINVAR