List of variants reported as likely pathogenic for autosomal recessive complex spastic paraplegia type 9B

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002860.4(ALDH18A1):c.2177G>A (p.Arg726His)	rs773714478	0.00004
NM_002860.4(ALDH18A1):c.1481C>T (p.Ala494Val)	rs762154638	0.00001
NM_002860.4(ALDH18A1):c.991A>C (p.Thr331Pro)	rs765380273	0.00001
NM_002860.4(ALDH18A1):c.1596_1600del (p.Val533fs)	rs2097844381
NM_002860.4(ALDH18A1):c.743G>A (p.Ser248Asn)	rs2097873418

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