Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs767796996
rs767796996
RAD51C
C 0.700 GeneticVariation CLINVAR The RAD51C exonic splice-site mutations c.404G>C and c.404G>T are associated with familial breast and ovarian cancer. 27622768

2017
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations. 25154786

2015
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Genetic testing for RAD51C mutations: in the clinic and community. 25470109

2015
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Pathological features of breast and ovarian cancers in RAD51C germline mutation carriers. 24993905

2014
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Germline mutations in RAD51C in Jewish high cancer risk families. 23117857

2012
dbSNP: rs767796996
rs767796996
RAD51C
A 0.700 GeneticVariation CLINVAR Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. 22451500

2012
dbSNP: rs767796996
rs767796996
RAD51C
C 0.700 GeneticVariation CLINVAR Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families. 22451500

2012