ClinVar Miner

Submissions for variant NM_207361.6(FREM2):c.7329T>A (p.Pro2443=)

dbSNP: rs1303270704
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) RCV000595047 SCV000702657 uncertain significance not provided 2016-11-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000595047 SCV004329639 likely benign not provided 2023-10-13 criteria provided, single submitter clinical testing

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