"DDHD1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2644242	NM_001160148.2(DDHD1):c.2508A>G (p.Lys836=)	DDHD1	Single nucleotide variant (synonymous variant +1 more)	DDHD1-related condition +1 more	GLikely benign
Select item 2080953	NM_001160148.2(DDHD1):c.2437+7T>G	DDHD1	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 28 +1 more	GLikely benign
Select item 464309	NM_001160148.2(DDHD1):c.2408A>G (p.His803Arg)	DDHD1 (H803R +1 more)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia +4 more	GConflicting classifications of pathogenicity
Select item 391795	NM_001160148.2(DDHD1):c.1890G>A (p.Ala630=)	DDHD1	Single nucleotide variant (synonymous variant)	Hereditary spastic paraplegia 28 +3 more	GBenign/Likely benign
Select item 1985180	NM_001160148.2(DDHD1):c.1527G>A (p.Glu509=)	DDHD1	Single nucleotide variant (synonymous variant)	DDHD1-related condition +1 more	GLikely benign
Select item 3036848	NM_001160148.2(DDHD1):c.342C>T (p.Ser114=)	DDHD1	Single nucleotide variant (synonymous variant)	DDHD1-related condition	GLikely benign
Select item 702126	NM_001160148.2(DDHD1):c.110G>C (p.Gly37Ala)	DDHD1 (G37A)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 28 +1 more	GLikely benign

ClinVar