DisGeNET - a database of gene-disease associations

Neoplastic Syndromes, Hereditary, C0027672

Variant: rs779582317 ×

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:

rs779582317

RAD51C ; LOC105371843

0.700

GeneticVariation

CLINVAR

Inherited Mutations in Women With Ovarian Carcinoma.

26720728

2016

dbSNP:

rs779582317

RAD51C ; LOC105371843

0.700

GeneticVariation

CLINVAR

Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer.

26824983

2016

dbSNP:

rs779582317

RAD51C ; LOC105371843

0.700

CausalMutation

CLINVAR

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

25470109

2015

dbSNP:

rs779582317

RAD51C ; LOC105371843

0.700

GeneticVariation

CLINVAR

Germline RAD51C mutations in ovarian cancer susceptibility.

22725699

2013

dbSNP:

rs779582317

RAD51C ; LOC105371843

0.700

CausalMutation

CLINVAR

Germline RAD51C mutations in ovarian cancer susceptibility.

22725699

2013