ClinVar Miner

List of variants in gene CADM3 reported as uncertain significance for Charcot-Marie-Tooth disease, axonal, type 2FF

Included ClinVar conditions (1):

Charcot-Marie-Tooth disease, axonal, type 2FF

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	gnomAD frequency
NM_001127173.3(CADM3):c.1000G>T (p.Gly334Cys)
NM_001127173.3(CADM3):c.1061A>G (p.Tyr354Cys)
NM_001127173.3(CADM3):c.383del

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