ClinVar Miner

Submissions for variant NM_015340.4(LARS2):c.2421G>A (p.Pro807=)

gnomAD frequency: 0.00006  dbSNP: rs777901333
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001534771 SCV001751724 likely benign not provided 2019-11-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001534771 SCV002390142 likely benign not provided 2024-10-17 criteria provided, single submitter clinical testing

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