ClinVar Miner

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

dbSNP: rs752087253
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Total submissions: 2
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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
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799041 SCV002041921 benign Cardiomyopathy 2019-08-14 criteria provided, single submitter clinical testing

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