ClinVar Miner

Submissions for variant NM_001540.5(HSPB1):c.110G>C (p.Arg37Pro)

dbSNP: rs372197630
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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 RCV001172561 SCV001335623 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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