ClinVar Miner

Submissions for variant NM_001379081.2(FREM1):c.5335-11del

dbSNP: rs140882884
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002118956 SCV002444089 benign not provided 2024-01-16 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494409 SCV002799071 likely benign Oculotrichoanal syndrome; BNAR syndrome; Trigonocephaly 2 2021-07-23 criteria provided, single submitter clinical testing

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