DisGeNET - a database of gene-disease associations

Neoplastic Syndromes, Hereditary, C0027672

Variant: rs730881942 ×

Source: CLINVAR ×

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:

rs730881942

RAD51C ; TEX14

0.700

CausalMutation

CLINVAR

Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.

26681312

2016

dbSNP:

rs730881942

RAD51C ; TEX14

0.700

CausalMutation

CLINVAR

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

27433846

2016

dbSNP:

rs730881942

RAD51C ; TEX14

0.700

CausalMutation

CLINVAR

Genetic testing for RAD51C mutations: in the clinic and community.

25470109

2015

dbSNP:

rs730881942

RAD51C ; TEX14

0.700

CausalMutation

CLINVAR

Screening of Finnish RAD51C founder mutations in prostate and colorectal cancer patients.

23176254

2012

dbSNP:

rs730881942

RAD51C ; TEX14

0.700

CausalMutation

CLINVAR

RAD51C is a susceptibility gene for ovarian cancer.

21616938

2011