DisGeNET - a database of gene-disease associations

rs730880868, MYH7

N. diseases: 1

Source: ALL

Results per page

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

N. SNPs_d

DSI _v

DPI _v

Chr

Position

Consequence

Alleles

Class

AF_EXOME

AF_GENOME

Score _vda

EI _vda

N. PMIDs

First Ref.

Last Ref.

Cardiomyopathy, Familial Hypertrophic, 1 (disorder)

CUI:	C3495498
Disease:	Cardiomyopathy, Familial Hypertrophic, 1 (disorder)

163

1.000

0.080

14

23429255

missense variant

C/T

snv

1.6E-05

1.4E-05

0.700