"PreventionGenetics, part of Exact Sciences"[submitter] AND "HSPB8"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 696431	NM_014365.3(HSPB8):c.171C>T (p.Ser57=)	HSPB8	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2L +1 more	GBenign/Likely benign
Select item 3036743	NM_014365.3(HSPB8):c.297T>C (p.Cys99=)	HSPB8	Single nucleotide variant (synonymous variant)	HSPB8-related disorder	GLikely benign
Select item 701838	NM_014365.3(HSPB8):c.309C>T (p.His103=)	HSPB8	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2L +1 more	GLikely benign
Select item 260402	NM_014365.3(HSPB8):c.402T>C (p.Ile134=)	HSPB8	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2L +3 more	GBenign
Select item 260403	NM_014365.3(HSPB8):c.582C>T (p.Thr194=)	HSPB8	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease axonal type 2L +3 more	GBenign
Select item 3030400	NM_014365.3(HSPB8):c.*881C>T	HSPB8	Single nucleotide variant (3 prime UTR variant)	HSPB8-related disorder	GLikely benign

ClinVar