ClinVar Miner

Submissions for variant NM_002693.3(POLG):c.3105-16_3105-15del

dbSNP: rs146915033
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000188521 SCV000843332 benign not specified 2020-04-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001519997 SCV001728973 benign Progressive sclerosing poliodystrophy 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV001706163 SCV001901716 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
GeneDx RCV000188521 SCV000242135 benign not specified 2013-04-16 flagged submission clinical testing The variant is found in EPILEPSY,INFANT-EPI,CHILD-EPI panel(s).

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