ClinVar Miner

Submissions for variant NM_021020.5(LZTS1):c.88C>A (p.His30Asn)

gnomAD frequency: 0.00245  dbSNP: rs145365423
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002176972 SCV002337153 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV002176972 SCV004236286 uncertain significance not provided 2021-04-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002176972 SCV005266542 benign not provided criteria provided, single submitter not provided

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