ClinVar Miner

Submissions for variant NM_001110556.2(FLNA):c.1061_1065del (p.His354fs)

dbSNP: rs786205180
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Claritas Genomics RCV000170400 SCV000222823 likely pathogenic Heterotopia, periventricular, X-linked dominant 2013-06-06 criteria provided, single submitter clinical testing

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