List of variants reported as likely benign for Spinocerebellar ataxia type 29; Spinocerebellar ataxia type 15/16; Gillespie syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001378452.1(ITPR1):c.1302G>A (p.Pro434=)	rs34252981	0.01036
NM_001378452.1(ITPR1):c.1554+17G>A	rs80123990	0.01028
NM_001378452.1(ITPR1):c.2433T>A (p.Ile811=)	rs145220403	0.00924
NM_001378452.1(ITPR1):c.7509T>C (p.Asp2503=)	rs79720149	0.00191
NM_001378452.1(ITPR1):c.3461A>G (p.Asp1154Gly)	rs61751570	0.00168
NM_001378452.1(ITPR1):c.4254G>T (p.Val1418=)	rs142527379	0.00107
NM_001378452.1(ITPR1):c.3945T>C (p.Asn1315=)	rs193212750	0.00051
NM_001378452.1(ITPR1):c.3669G>A (p.Val1223=)	rs201263269	0.00014
NM_001378452.1(ITPR1):c.3705C>T (p.Ala1235=)	rs34635052

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