"HSPD1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2633904	NM_002156.5(HSPD1):c.1612_1613del (p.Leu538fs)	HSPD1 (L538fs)	Microsatellite (frameshift variant)	HSPD1-related condition	GUncertain significance
Select item 701949	NM_002156.5(HSPD1):c.750A>G (p.Lys250=)	HSPD1	Single nucleotide variant (synonymous variant)	Spastic paraplegia +1 more	GLikely benign
Select item 695547	NM_002156.5(HSPD1):c.700+8C>T	HSPD1	Single nucleotide variant (intron variant)	Spastic paraplegia +3 more	GBenign/Likely benign
Select item 214549	NM_002156.5(HSPD1):c.561T>C (p.Ser187=)	HSPD1	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 13 +6 more	GBenign/Likely benign
Select item 3050846	NM_002156.5(HSPD1):c.477T>G (p.Ser159=)	HSPD1	Single nucleotide variant (synonymous variant)	HSPD1-related condition	GLikely benign
Select item 2630153	NM_002156.5(HSPD1):c.188T>C (p.Ile63Thr)	HSPD1 (I63T)	Single nucleotide variant (missense variant)	HSPD1-related condition	GLikely pathogenic
Select item 129242	NM_002156.5(HSPD1):c.27C>G (p.Arg9=)	HSPD1	Single nucleotide variant (synonymous variant)	HSPD1-related condition +5 more	GConflicting classifications of pathogenicity

ClinVar