List of variants reported as uncertain significance for Spinocerebellar ataxia type 29; Spinocerebellar ataxia type 15/16; Gillespie syndrome

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001378452.1(ITPR1):c.3664G>A (p.Ala1222Thr)	rs372881053	0.00006
NM_001378452.1(ITPR1):c.7474G>A (p.Gly2492Ser)	rs187571979	0.00006
NM_001378452.1(ITPR1):c.6817G>A (p.Val2273Met)	rs767779223	0.00002
NM_001378452.1(ITPR1):c.3199G>A (p.Gly1067Ser)	rs776099053	0.00001
NM_001378452.1(ITPR1):c.1252-10T>A	rs2125191741
NM_001378452.1(ITPR1):c.5140C>A (p.Pro1714Thr)
NM_001378452.1(ITPR1):c.7648G>A (p.Gly2550Arg)	rs1553757628
NM_001378452.1(ITPR1):c.805C>T (p.Arg269Trp)	rs886039392

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