List of variants in gene HSPB8 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014365.3(HSPB8):c.707_720delinsAAAA	rs886049028
NM_014365.3(HSPB8):c.*848TAA[10]	rs60924821
NM_014365.3(HSPB8):c.*848TAA[9]	rs60924821

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