ClinVar Miner

Submissions for variant NM_007215.4(POLG2):c.1111-20dup

dbSNP: rs1555666811
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000480191 SCV000569274 likely benign not specified 2016-02-23 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002063729 SCV002379783 benign not provided 2023-10-27 criteria provided, single submitter clinical testing

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