ClinVar Miner

Submissions for variant NM_000530.8(MPZ):c.645+10A>G

dbSNP: rs1670232533
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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 RCV001174334 SCV001337470 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002559672 SCV003447953 likely benign Charcot-Marie-Tooth disease, type I 2022-08-22 criteria provided, single submitter clinical testing

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