| Submitter |
RCV |
SCV |
Clinical significance |
Condition |
Last evaluated |
Review status |
Method |
Comment |
| Fulgent Genetics, Fulgent Genetics |
RCV005017746 |
SCV005644356 |
uncertain significance |
Familial cancer of breast; Blepharocheilodontic syndrome 1; Endometrial carcinoma; Hereditary diffuse gastric adenocarcinoma; Ovarian cancer |
2024-02-08 |
criteria provided, single submitter |
clinical testing |
|
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