DisGeNET - a database of gene-disease associations

RAD51C, RAD51 paralog C, 5889

N. diseases: 162; N. variants: 96

Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP O ×

Variant: rs730881942 ×

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs730881942

Entrez Id:	5889;56155
Gene Symbol:	RAD51C;TEX14

RAD51C;TEX14

CUI:	C3150653
Disease:

FANCONI ANEMIA, COMPLEMENTATION GROUP O

0.700

CausalMutation

CLINVAR

Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.

27433846

2016

dbSNP:

rs730881942

Entrez Id:	5889;56155
Gene Symbol:	RAD51C;TEX14

RAD51C;TEX14

CUI:	C3150653
Disease:

FANCONI ANEMIA, COMPLEMENTATION GROUP O

0.700

CausalMutation

CLINVAR

Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan.

24800917

2014

dbSNP:

rs730881942

Entrez Id:	5889;56155
Gene Symbol:	RAD51C;TEX14

RAD51C;TEX14

CUI:	C3150653
Disease:

FANCONI ANEMIA, COMPLEMENTATION GROUP O

0.700

CausalMutation

CLINVAR

RAD51C is a susceptibility gene for ovarian cancer.

21616938

2011