ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.572T>G (p.Val191Gly)

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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 RCV001172627 SCV001335690 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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