ClinVar Miner

Submissions for variant NM_015340.4(LARS2):c.1392C>T (p.Cys464=)

gnomAD frequency: 0.00014  dbSNP: rs775041032
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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
GeneDx RCV001704697 SCV000713959 likely benign not provided 2021-06-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001704697 SCV003494814 likely benign not provided 2024-11-25 criteria provided, single submitter clinical testing

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