ClinVar Miner

Submissions for variant NM_000304.4(PMP22):c.*985C>T (rs886052610)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000366590 SCV000400689 uncertain significance Hereditary liability to pressure palsies 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000269664 SCV000400690 uncertain significance Charcot-Marie-Tooth disease, type I 2016-06-14 criteria provided, single submitter clinical testing

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