ClinVar Miner

Submissions for variant NC_000002.12:g.(?_47614711)_(47657080_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Personalized Medicine Clinic, Tartu University Hospital RCV003229522 SCV003925768 likely pathogenic Lynch syndrome 1 no assertion criteria provided clinical testing Colorectal cancer in anamnesis. The identical twin brother had Colorectal cancer, the father had a brain tumour, and mother`s mother had an unknown tumour of the stomach.

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