ClinVar Miner

Submissions for variant NM_006017.3(PROM1):c.879C>T (p.Ser293=)

dbSNP: rs148242593
Minimum review status: Collection method:
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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
Eurofins Ntd Llc (ga) RCV000180293 SCV000232701 uncertain significance not provided 2015-02-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000180293 SCV001723106 benign not provided 2023-12-25 criteria provided, single submitter clinical testing

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