List of variants studied for spinocerebellar ataxia, autosomal recessive, with axonal neuropathy by Fulgent Genetics, Fulgent Genetics

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_015046.7(SETX):c.59G>A (p.Arg20His)	rs79740039	0.00602
NM_015046.7(SETX):c.4755T>G (p.Pro1585=)	rs151237267	0.00484
NM_015046.7(SETX):c.4982C>G (p.Pro1661Arg)	rs146873848	0.00080
NM_015046.7(SETX):c.3826C>G (p.Gln1276Glu)	rs148604312	0.00039
NM_015046.7(SETX):c.654G>C (p.Lys218Asn)	rs117861188	0.00039
NM_015046.7(SETX):c.7432A>G (p.Thr2478Ala)	rs142303658	0.00038
NM_015046.7(SETX):c.4433C>A (p.Ala1478Glu)	rs143661911	0.00034
NM_015046.7(SETX):c.5536C>T (p.Arg1846Cys)	rs551406712	0.00007
NM_015046.7(SETX):c.3016G>A (p.Gly1006Arg)	rs141266068	0.00006
NM_015046.7(SETX):c.4865C>T (p.Pro1622Leu)	rs140781535	0.00005
NM_015046.7(SETX):c.4828C>T (p.Leu1610Phe)	rs749891883	0.00004
NM_015046.7(SETX):c.1989_1994del (p.Ile664_Glu665del)	rs773195802	0.00001
NM_015046.7(SETX):c.71A>G (p.Asn24Ser)	rs981346599	0.00001
NM_018319.4(TDP1):c.1317G>T (p.Leu439Phe)	rs138711165

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