DisGeNET - a database of gene-disease associations

CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder), C2748542

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

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs121434627

rs121434627

SCN1B

C

0.700

CausalMutation

CLINVAR

dbSNP:

rs137854612

rs137854612

SCN5A

T

0.700

CausalMutation

CLINVAR

dbSNP:

rs267607029

rs267607029

SCN1B

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs869025458

rs869025458

LMNA

AG

0.700

GeneticVariation

CLINVAR