ClinVar Miner

Submissions for variant NM_015965.7(NDUFA13):c.45C>A (p.Gly15=)

gnomAD frequency: 0.00038  dbSNP: rs183288709
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000299323 SCV000333235 uncertain significance not provided 2015-07-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000299323 SCV003258033 likely benign not provided 2025-01-07 criteria provided, single submitter clinical testing

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