ClinVar Miner

Submissions for variant NM_000228.3(LAMB3):c.1455G>A (p.Pro485=)

gnomAD frequency: 0.00001  dbSNP: rs1033335294
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000976521 SCV001124425 likely benign not provided 2024-11-21 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000976521 SCV003816414 uncertain significance not provided 2019-03-23 criteria provided, single submitter clinical testing

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