ClinVar Miner

Submissions for variant NM_001457.4(FLNB):c.3724+13_3724+15del

gnomAD frequency: 0.00809  dbSNP: rs773897420
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000290637 SCV000445734 uncertain significance FLNB-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001555305 SCV001776697 likely benign not provided 2019-10-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001555305 SCV002385409 likely benign not provided 2025-01-27 criteria provided, single submitter clinical testing

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