ClinVar Miner

Submissions for variant NM_002693.3(POLG):c.-200del

dbSNP: rs150780058
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000380618 SCV000394303 likely benign POLG-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001672517 SCV001885956 benign not provided 2021-04-08 criteria provided, single submitter clinical testing

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