ClinVar Miner

Submissions for variant NM_001493.3(GDI1):c.1237A>G (p.Thr413Ala)

dbSNP: rs1569553475
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes RCV000782056 SCV000920525 likely benign not provided 2019-02-06 criteria provided, single submitter clinical testing

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