ClinVar Miner

Submissions for variant NM_005340.7(HINT1):c.111+5_111+6insC (rs1580686330)

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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 RCV001000912 SCV001157998 benign Autosomal recessive axonal neuropathy with neuromyotonia 2018-11-27 criteria provided, single submitter clinical testing

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