List of variants in gene GDAP1 reported as uncertain significance for Autosomal dominant Charcot-Marie-Tooth disease type 2K

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_018972.4(GDAP1):c.678A>C (p.Arg226Ser)	rs267606842
NM_018972.4(GDAP1):c.678A>T (p.Arg226Ser)	rs267606842
NM_018972.4(GDAP1):c.719G>A (p.Cys240Tyr)	rs121908115

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