Submissions for variant NM_002047.4(GARS1):c.332C>T (p.Ala111Val) (rs370531212)

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
Inherited Neuropathy Consortium	RCV000789053	SCV000928402	uncertain significance	Charcot-Marie-Tooth disease		no assertion criteria provided	literature only
Inherited Neuropathy Consortium	RCV000790252	SCV000929651	uncertain significance	Distal spinal muscular atrophy		no assertion criteria provided	literature only

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