ClinVar Miner

Submissions for variant NM_001379081.2(FREM1):c.6021C>G (p.Pro2007=)

gnomAD frequency: 0.00030  dbSNP: rs200987019
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
Eurofins Ntd Llc (ga) RCV000349900 SCV000336287 uncertain significance not provided 2015-10-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000349900 SCV003270687 likely benign not provided 2024-05-27 criteria provided, single submitter clinical testing

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