List of variants in gene SPAST reported as likely pathogenic for Inborn genetic diseases

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_014946.4(SPAST):c.1032A>G (p.Ile344Met)	rs2465839683
NM_014946.4(SPAST):c.1206CTT[1] (p.Phe404del)	rs1553317028
NM_014946.4(SPAST):c.1459A>G (p.Asn487Asp)	rs1553318323
NM_014946.4(SPAST):c.1496G>A (p.Arg499His)	rs878854991
NM_014946.4(SPAST):c.1634C>G (p.Ser545Ter)	rs869312949
NM_014946.4(SPAST):c.1823dup (p.Asn608fs)	rs2465946676

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