List of variants reported as likely benign for Spinocerebellar ataxia type 35 by Illumina Laboratory Services, Illumina

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_198994.3(TGM6):c.-2A>G	rs80329336	0.00475
NM_198994.3(TGM6):c.1011G>A (p.Glu337=)	rs142832802	0.00056
NM_198994.3(TGM6):c.1452C>T (p.Asp484=)	rs142748417	0.00046
NM_198994.3(TGM6):c.622G>A (p.Val208Met)	rs61743614	0.00037
NM_198994.3(TGM6):c.1690C>T (p.Pro564Ser)	rs200674917	0.00034
NM_198994.3(TGM6):c.277A>G (p.Met93Val)	rs146529216	0.00029
NM_198994.3(TGM6):c.38G>A (p.Arg13Gln)	rs201694328	0.00027
NM_198994.3(TGM6):c.-42C>T	rs376489998	0.00016
NM_198994.3(TGM6):c.379C>T (p.Arg127Trp)	rs148854519	0.00014
NM_198994.3(TGM6):c.951C>T (p.Phe317=)	rs201333931	0.00010
NM_198994.3(TGM6):c.595G>A (p.Gly199Ser)	rs182249285	0.00004
NM_198994.3(TGM6):c.621C>A (p.Asp207Glu)	rs148696208	0.00003
NM_198994.3(TGM6):c.717G>A (p.Gln239=)	rs201506281	0.00002
NM_198994.3(TGM6):c.850+4C>T	rs765181893	0.00002
NM_198994.3(TGM6):c.1478C>T (p.Pro493Leu)	rs776319756	0.00001
NM_198994.3(TGM6):c.390C>T (p.Gly130=)	rs751704232	0.00001
NM_198994.3(TGM6):c.1653C>T (p.His551=)	rs755072071
NM_198994.3(TGM6):c.303C>T (p.Leu101=)	rs757250219

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