List of variants in gene DDHD1 reported as likely benign for Hereditary spastic paraplegia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001160148.2(DDHD1):c.1524A>G (p.Gln508=)	rs138906273	0.00150
NM_001160148.2(DDHD1):c.1890G>A (p.Ala630=)	rs546774166	0.00002
NM_001160148.2(DDHD1):c.181G>C (p.Gly61Arg)	rs568294049	0.00001
NM_001160148.2(DDHD1):c.1993-19dup	rs755741246

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