List of variants in gene ARHGEF10 reported as uncertain significance for Charcot-Marie-Tooth disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP
NM_014629.4(ARHGEF10):c.1110G>C (p.Leu370Phe)	rs9657362
NM_014629.4(ARHGEF10):c.2197C>T (p.His733Tyr)	rs147531758
NM_014629.4(ARHGEF10):c.604A>C (p.Asn202His)	rs767902219

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