ClinVar Miner

Submissions for variant NM_003849.4(SUCLG1):c.98-14_98-11del

dbSNP: rs56733272
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000505994 SCV000605318 benign Mitochondrial DNA depletion syndrome 9 2023-11-29 criteria provided, single submitter clinical testing
GeneDx RCV000677033 SCV001941522 benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000505994 SCV002408823 benign Mitochondrial DNA depletion syndrome 9 2024-01-08 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000677033 SCV000802867 likely benign not provided 2017-08-08 no assertion criteria provided clinical testing

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