DisGeNET - a database of gene-disease associations

hearing impairment, C1384666

Gene: ERCC2 ×

Source: INFERRED ×

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:

rs1568546120

rs1568546120

ERCC2

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs1568546252

rs1568546252

ERCC2

A

0.700

CausalMutation

CLINVAR

dbSNP:

rs964247601

rs964247601

ERCC2

A

0.700

CausalMutation

CLINVAR