ClinVar Miner

Submissions for variant NM_138361.5(LRSAM1):c.528+15G>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory,London Health Sciences Centre RCV001172648 SCV001335711 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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