ClinVar Miner

Submissions for variant NM_000304.4(PMP22):c.206T>G (p.Met69Arg) (rs104894620)

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Inherited Neuropathy Consortium	RCV000790164	SCV000929555	uncertain significance	Charcot-Marie-Tooth disease		no assertion criteria provided	literature only

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