ClinVar Miner

Submissions for variant NM_138361.5(LRSAM1):c.619+14G>A (rs770398029)

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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 RCV001002393 SCV001160314 likely benign Charcot-Marie-Tooth disease type 2P 2019-02-15 criteria provided, single submitter clinical testing

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