List of variants reported as uncertain significance for Autosomal recessive ataxia, Beauce type by Baylor Genetics

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_182961.4(SYNE1):c.14452T>A (p.Tyr4818Asn)	rs142422990	0.00101
NM_182961.4(SYNE1):c.21995A>C (p.His7332Pro)	rs151247098	0.00080
NM_182961.4(SYNE1):c.3536A>C (p.Glu1179Ala)	rs117461489	0.00057
NM_182961.4(SYNE1):c.12667C>T (p.Arg4223Cys)	rs145738035	0.00006
NM_182961.4(SYNE1):c.334A>T (p.Thr112Ser)	rs750010888	0.00006
NM_182961.4(SYNE1):c.13918T>C (p.Tyr4640His)	rs748256440	0.00003
NM_182961.4(SYNE1):c.14634A>C (p.Glu4878Asp)	rs1159750019	0.00001
NM_182961.4(SYNE1):c.21077A>C (p.Glu7026Ala)	rs777755452	0.00001
NM_182961.4(SYNE1):c.8532G>A (p.Met2844Ile)	rs794727764	0.00001
NM_182961.4(SYNE1):c.8984T>C (p.Ile2995Thr)	rs527822279	0.00001
NM_182961.4(SYNE1):c.17483C>G (p.Thr5828Arg)	rs150376715
NM_182961.4(SYNE1):c.18409G>A (p.Val6137Met)	rs945540285
NM_182961.4(SYNE1):c.18964G>C (p.Glu6322Gln)	rs376472604
NM_182961.4(SYNE1):c.9821G>A (p.Arg3274Lys)	rs2097100149

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