List of variants in gene RAB7A reported as uncertain significance for Charcot-Marie-Tooth disease type 2

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004637.5(RAB7A):c.-209_-204dup	rs770559386
NM_004637.6(RAB7A):c.*182CA[9]	rs139417205
NM_004637.6(RAB7A):c.421_423del	rs886057944
NM_004637.6(RAB7A):c.*801dup	rs886057948
NM_004637.6(RAB7A):c.-70CTC[2]	rs763539443

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