ClinVar Miner

Submissions for variant NM_001110556.2(FLNA):c.2466C>T (p.Ile822=)

gnomAD frequency: 0.00001  dbSNP: rs878854461
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001392128 SCV001593762 likely benign Heterotopia, periventricular, X-linked dominant; Melnick-Needles syndrome; Oto-palato-digital syndrome, type II; Frontometaphyseal dysplasia 2022-11-10 criteria provided, single submitter clinical testing

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