ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.10995G>A (p.Gly3665=)

gnomAD frequency: 0.00001  dbSNP: rs572991122
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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 RCV001173875 SCV001336991 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068098 SCV002395758 likely benign Charcot-Marie-Tooth disease axonal type 2O 2022-11-23 criteria provided, single submitter clinical testing

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