List of diseases covered by
Breast and Ovarian Cancer NGS panel
Gene | Condition |
ATM | Ataxia-telangiectasia; Breast cancer, susceptibility to |
BARD1 | Breast cancer, susceptibility to |
BRCA1 | Breast-ovarian cancer, familial, 1; Pancreatic cancer, susceptibility to, 4; Fanconi anemia, complementation group S |
BRCA2 | Fanconi anemia, complementation group D1; Wilms tumor; Breast cancer, male, susceptibility to; Breast-ovarian cancer, familial, 2; Glioblastoma 3; Medulloblastoma; Pancreatic cancer 2; Prostate cancer |
BRIP1 | Breast cancer, early-onset; Fanconi anemia, complementation group J |
CDH1 | Breast cancer, lobular; Prostate cancer, susceptibility to; Endometrial carcinoma, somatic; Ovarian carcinoma, somatic; Blepharocheilodontic syndrome 1; Gastric cancer, familial diffuse, with or without cleft lip and/or palate< |
CHEK2 | Breast cancer, susceptibility to; Prostate cancer, familial, susceptibility to; Li-Fraumeni syndrome; Osteosarcoma, somatic |
MEN1 | Multiple endocrine neoplasia 1 |
MLH1 | Mismatch repair cancer syndrome; Colorectal cancer, hereditary nonpolyposis, type 2; Muir-Torre syndrome |
MRE11A | Ataxia-telangiectasia-like disorder 1 |
MSH2 | Mismatch repair cancer syndrome; Colorectal cancer, hereditary nonpolyposis, type 1; Muir-Torre syndrome |
MSH6 | Mismatch repair cancer syndrome; Colorectal cancer, hereditary nonpolyposis, type 5; Endometrial cancer, familial |
MUTYH | Adenomas, multiple colorectal; Colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas; Gastric cancer, somatic |
NBN | Nijmegen breakage syndrome; Leukemia, acute lymphoblastic; Aplastic anemia |
PALB2 | Breast cancer, susceptibility to; Pancreatic cancer, susceptibility to, 3; Fanconi anemia, complementation group N |
PTCH1 | Basal cell nevus syndrome; Holoprosencephaly 7; Basal cell carcinoma, somatic |
PTEN | Glioma susceptibility 2, Meningioma, Macrocephaly/autism syndrome; Endometrial carcinoma, somatic; Malignant melanoma, somatic; Squamous cell carcinoma, head and neck, somatic; Prostate cancer, somatic; VATER association with macrocephaly and ventriculomegaly; Bannayan-Riley-Ruvalcaba syndrome; Cowden syndrome 1 |
RAD50 | Nijmegen breakage syndrome-like disorder |
RAD51C | Breast-ovarian cancer, familial, susceptibility to, 3; Fanconi anemia, complementation group O |
RAD51D | Breast-ovarian cancer, familial, susceptibility to, 4 |
STK11 | Pancreatic cancer; Peutz-Jeghers syndrome; Testicular tumor, somatic |
TP53 | Breast cancer; Adrenal cortical carcinoma; Choroid plexus papilloma; Colorectal cancer; Li-Fraumeni syndrome; Nasopharyngeal carcinoma; Osteosarcoma; Pancreatic cancer; Basal cell carcinoma 7; Glioma susceptibility 1 |
XRCC2 | Fanconi anemia, complementation group U |