ClinVar Miner

Submissions for variant PMP22, 1.1- to 1.5-MB DEL

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000008942 SCV000029152 pathogenic Hereditary liability to pressure palsies 2011-06-01 no assertion criteria provided literature only
OMIM RCV000008943 SCV000053461 pathogenic Polyneuropathy, inflammatory demyelinating 2011-06-01 no assertion criteria provided literature only
OMIM RCV000008944 SCV000053462 pathogenic Autosomal recessive Dejerine-Sottas syndrome 2011-06-01 no assertion criteria provided literature only

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