ClinVar Miner

Submissions for variant NM_003172.4(SURF1):c.552G>A (p.Arg184=)

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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 RCV002780752 SCV003019723 likely benign Leigh syndrome 2022-09-05 criteria provided, single submitter clinical testing

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