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BRCA1 mutation carriers (1)
BRCA1 mutations (1)
BRCA2 mutation carriers (1)
BRCA2 mutations (1)
BRCA2-Specific Modifier Locus at 6p24 (1)
Breast cancer (BC) (1)
Breast cancer subtype (1)
Breast carcinogenesis (1)
Cancer epidemiology (1)
Cancer genetics (1)
Cancer risk in carriers (1)
Candidate genetic modifiers (1)
Carriers (1)
Causal gene (1)
CCDC91 (1)
Coiled-coil domain containing 170 (CCDC170) (1)
Disease susceptibility (1)
Epidemiology (1)
ER-negative breast cancer (1)
Estrogen Receptor 1 (ESR1) (1)
Ethnicity (1)
Fine-scale mapping (1)
Founder mutations (1)
Genes (1)
Genetic factors (1)
Genetic risk factor (1)
Genetics (1)
Geography (1)
Germline mutations (1)
Haplotype studies (1)
Height (1)
Hereditary breast and ovarian cancer (1)
Hereditary breast cancer (1)
Hispanics (1)
Invasive (1)
Locus (1)
Mendelian randomisation (1)
Mitochondria (1)
Mutation (1)
Mutation carriers (1)
Ovarian cancer (OC) (1)
Pathogenic mutations (1)
Pathogenic sequence variant (PSV) (1)
Polygenic risk scores (PRS) (1)
Prediction (1)
Prostate cancer (1)
PTHLH (1)
Required for meiotic nuclear division 1 (RMND1) (1)
Risk factors (1)
SDG-03: Good health and well-being (1)
Transcriptome-wide association studies (TWAS) (1)
Transheterozygosity (1)
Transheterozygotes (TH) (1)
Type and location (1)
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