ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.4370T>C (p.Met1457Thr) (rs1567006359)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Institute of Human Genetics,University of Goettingen	RCV000767219	SCV000897613	uncertain significance	Charcot-Marie-Tooth disease, axonal, type 2O	2019-03-29	no assertion criteria provided	clinical testing

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