ClinVar Miner

Submissions for variant NM_001370298.3(FGD4):c.1824T>G (p.Val608=)

dbSNP: rs1949688594
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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 RCV001174103 SCV001337224 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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