ClinVar Miner

Submissions for variant NM_138361.5(LRSAM1):c.1632G>A (p.Gln544=) (rs762712712)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000649940 SCV000771776 likely benign Charcot-Marie-Tooth disease type 2P 2017-12-26 criteria provided, single submitter clinical testing

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