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Peer Review reports

From: Occurrence of variants of unknown clinical significance in genetic testing for hereditary breast and ovarian cancer syndrome and Lynch syndrome: a literature review and analytical observational retrospective cohort study

Original Submission
25 Jul 2022 Submitted Original manuscript
27 Sep 2022 Reviewed Reviewer Report - Andreas Laner
14 Oct 2022 Reviewed Reviewer Report
19 Oct 2022 Reviewed Reviewer Report
4 Nov 2022 Author responded Author comments - Manuela Rabaglio
Resubmission - Version 2
4 Nov 2022 Submitted Manuscript version 2
14 Nov 2022 Author responded Author comments - Manuela Rabaglio
Resubmission - Version 3
14 Nov 2022 Submitted Manuscript version 3
22 Nov 2022 Reviewed Reviewer Report - Andreas Laner
7 Dec 2022 Reviewed Reviewer Report
8 Dec 2022 Reviewed Reviewer Report
14 Dec 2022 Author responded Author comments - Manuela Rabaglio
Resubmission - Version 4
14 Dec 2022 Submitted Manuscript version 4
15 Dec 2022 Author responded Author comments - Manuela Rabaglio
Resubmission - Version 5
15 Dec 2022 Submitted Manuscript version 5
Publishing
9 Jan 2023 Editorially accepted
16 Jan 2023 Article published 10.1186/s12920-023-01437-7

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