Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000115551 | SCV000149460 | uncertain significance | Hereditary cancer-predisposing syndrome | 2013-12-31 | criteria provided, single submitter | clinical testing | Deletion of 26 nucleotides in the PTEN promoter region; Not been published as a mutation or a benign polymorphism. This variant is found in BR-OV-HEREDIC panel(s). |