ClinVar Miner

Submissions for variant NC_000010.11:g.(?_87960841)_(87960878_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000204221 SCV000260938 benign PTEN hamartoma tumor syndrome 2015-11-09 criteria provided, single submitter clinical testing

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