List of variants reported as likely pathogenic for hereditary spastic paraplegia by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_025137.4(SPG11):c.733_734del (p.Met245fs)	rs312262720	0.00005
NM_014946.4(SPAST):c.631G>A (p.Val211Ile)	rs143003434	0.00002
NM_001122955.4(BSCL2):c.461C>T (p.Ser154Leu)	rs137852973	0.00001
NM_000533.5(PLP1):c.365A>G (p.Lys122Arg)	rs1135401759

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