DisGeNET - a database of gene-disease associations

Neoplastic Syndromes, Hereditary, C0027672

Variant: rs387907159 ×

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:

rs387907159

RAD51C

0.700

CausalMutation

CLINVAR

Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.

28281021

2017

dbSNP:

rs387907159

RAD51C

0.700

CausalMutation

CLINVAR

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

25470109

2015

dbSNP:

rs387907159

RAD51C

0.700

CausalMutation

CLINVAR

Germline RAD51C mutations confer susceptibility to ovarian cancer.

22538716

2012

dbSNP:

rs387907159

RAD51C

0.700

CausalMutation

CLINVAR

Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients.

21990120

2012

dbSNP:

rs387907159

RAD51C

0.700

CausalMutation

CLINVAR

Germline mutations in RAD51C in Jewish high cancer risk families.

23117857

2012