Submissions for variant NM_014874.4(MFN2):c.272T>G (p.Val91Gly) (rs1569816262)

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

Total submissions: 2

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Genesis Genome Database	RCV000857090	SCV000999663	uncertain significance	Charcot-Marie-Tooth disease	2019-08-14	no assertion criteria provided	research
Inherited Neuropathy Consortium	RCV000857090	SCV001190038	likely pathogenic	Charcot-Marie-Tooth disease		no assertion criteria provided	research

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