ClinVar Miner

Submissions for variant NM_138361.5(LRSAM1):c.814C>T (p.Arg272Trp) (rs149456922)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000863251 SCV001003881 likely benign Charcot-Marie-Tooth disease type 2P 2019-12-31 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173644 SCV001336746 uncertain significance Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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