DisGeNET - a database of gene-disease associations

Mild hearing impairment, C4022758

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:

rs111033258

rs111033258

CLRN1 ; CLRN1-AS1

C

0.700

CausalMutation

CLINVAR

dbSNP:

rs111033437

rs111033437

MYO7A

A

0.700

GeneticVariation

CLINVAR

dbSNP:

rs368869806

rs368869806

PTCH1

T

0.700

CausalMutation

CLINVAR

dbSNP:

rs387906271

rs387906271

CHD7

C

0.700

CausalMutation

CLINVAR