ClinVar Miner

Submissions for variant NM_139241.3(FGD4):c.93-20C>G (rs1592293275)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001002524 SCV001160485 likely benign Charcot-Marie-Tooth disease, type 4H 2019-05-01 criteria provided, single submitter clinical testing

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