ClinVar Miner

Submissions for variant NM_003849.4(SUCLG1):c.98-17_98-11del

dbSNP: rs56733272
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002531383 SCV002938186 likely benign Mitochondrial DNA depletion syndrome 9 2022-10-21 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000677034 SCV000802868 likely benign not provided 2016-03-16 no assertion criteria provided clinical testing

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