ClinVar Miner

Submissions for variant NM_001110556.2(FLNA):c.2609A>G (p.His870Arg) (rs200679107)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000715585 SCV000846414 likely benign History of neurodevelopmental disorder 2018-02-12 criteria provided, single submitter clinical testing Other strong data supporting benign classification;Other strong data
Gharavi Laboratory,Columbia University RCV000723221 SCV000854352 uncertain significance not provided 2018-09-16 no assertion criteria provided research

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