DisGeNET - a database of gene-disease associations

DEAFNESS, AUTOSOMAL RECESSIVE 66, C1857750

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:

rs794729665

rs794729665

DCDC2

0.800

GeneticVariation

UNIPROT

dbSNP:

rs794729665

rs794729665

DCDC2

G

0.800

CausalMutation

CLINVAR

dbSNP:

rs904944428

rs904944428

DCDC2

AT

0.700

CausalMutation

CLINVAR

Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis.

2016