"DNAJC17-related condition"[Disease/phenotype] AND "PreventionGenetics - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2896215	NM_018163.3(DNAJC17):c.855C>G (p.Ala285=)	DNAJC17	Single nucleotide variant (synonymous variant)	DNAJC17-related condition +1 more	GLikely benign
Select item 1554560	NM_018163.3(DNAJC17):c.669C>T (p.Thr223=)	DNAJC17	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1640998	NM_018163.3(DNAJC17):c.610G>C (p.Val204Leu)	DNAJC17 (V204L)	Single nucleotide variant (missense variant)	DNAJC17-related condition +1 more	GBenign/Likely benign
Select item 1616873	NM_018163.3(DNAJC17):c.576C>T (p.Asp192=)	DNAJC17	Single nucleotide variant (synonymous variant)	DNAJC17-related condition +1 more	GBenign
Select item 1549544	NM_018163.3(DNAJC17):c.495T>C (p.Thr165=)	DNAJC17	Single nucleotide variant (synonymous variant)	DNAJC17-related condition +1 more	GLikely benign
Select item 1601221	NM_018163.3(DNAJC17):c.463G>A (p.Asp155Asn)	DNAJC17 (D155N)	Single nucleotide variant (missense variant)	DNAJC17-related condition +1 more	GBenign
Select item 1588214	NM_018163.3(DNAJC17):c.350A>C (p.Glu117Ala)	DNAJC17 (E117A)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign

ClinVar