ClinVar Miner

Submissions for variant NM_002693.2(POLG):c.3105-16_3105-15delGT (rs146915033)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000188521 SCV000242135 benign not specified 2013-04-16 criteria provided, single submitter clinical testing The variant is found in EPILEPSY,INFANT-EPI,CHILD-EPI panel(s).
Athena Diagnostics Inc RCV000712801 SCV000843332 likely benign not provided 2018-03-08 criteria provided, single submitter clinical testing

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