DisGeNET - a database of gene-disease associations

rs730880289, DES

N. diseases: 1

Disease: MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED ×

Source: ALL

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED

CUI:	C1832370
Disease:	MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED

0.700

CausalMutation

CLINVAR

A dysfunctional desmin mutation in a patient with severe generalized myopathy.

1998