ClinVar Miner

Submissions for variant NM_001110556.2(FLNA):c.623-8C>A

dbSNP: rs111542756
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology RCV001262009 SCV001439373 uncertain significance Melnick-Needles syndrome 2020-08-26 criteria provided, single submitter research ACMG codes:PM2, PP3

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