ClinVar Miner

Submissions for variant NM_021020.5(LZTS1):c.1423C>G (p.Leu475Val)

gnomAD frequency: 0.06265  dbSNP: rs723874
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001656006 SCV001861720 benign not provided 2020-11-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001656006 SCV002403623 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001656006 SCV005266532 benign not provided criteria provided, single submitter not provided

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