Related gene-specific medical variations for Gene (Select 26353) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3360726	NM_014365.3(HSPB8):c.278G>A (p.Gly93Glu)	HSPB8 (G93E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2432542	NM_014365.3(HSPB8):c.539G>A (p.Ser180Asn)	HSPB8 (S180N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1806992	NM_014365.3(HSPB8):c.175G>A (p.Ala59Thr)	HSPB8 (A59T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1806991	NM_014365.3(HSPB8):c.138C>T (p.Ala46=)	HSPB8	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 931761	NM_014365.3(HSPB8):c.367+57del	HSPB8	Deletion (intron variant)	Charcot-Marie-Tooth disease axonal type 2L	GUncertain significance
Select item 694838	NM_014365.3(HSPB8):c.25T>C (p.Ser9Pro)	HSPB8 (S9P)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease	GUncertain significance

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