ClinVar Miner

Submissions for variant NM_020956.2(PRX):c.*1783G>A (rs567690884)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000654207 SCV000776097 likely benign Charcot-Marie-Tooth disease type 4 2019-12-31 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001172774 SCV001335842 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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