List of variants reported as likely benign for Charlevoix-Saguenay spastic ataxia by Illumina Laboratory Services, Illumina

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_000231.3(SGCG):c.705T>C (p.Leu235=)	rs1800353	0.60006
NM_000231.3(SGCG):c.*295T>C	rs3829352	0.37163
NM_014363.6(SACS):c.*484T>C	rs4770433	0.36808
NM_014363.6(SACS):c.9981T>C (p.Ala3327=)	rs2737700	0.36123
NM_000231.3(SGCG):c.*254G>A	rs3751371	0.31172
NM_014363.6(SACS):c.-13A>G	rs17078720	0.27905
NM_014363.6(SACS):c.6195T>C (p.Ile2065=)	rs4143768	0.21785
NM_014363.6(SACS):c.8853T>C (p.Val2951=)	rs9552929	0.21755
NM_014363.6(SACS):c.10106T>C (p.Val3369Ala)	rs17078605	0.21747
NM_014363.6(SACS):c.12304T>C (p.Leu4102=)	rs2737699	0.21736
NM_014363.6(SACS):c.171+6C>T	rs3751368	0.13441
NM_014363.6(SACS):c.696T>A (p.Asn232Lys)	rs2031640	0.08558
NM_014363.6(SACS):c.1656A>G (p.Leu552=)	rs1536365	0.08543
NM_000231.3(SGCG):c.*13C>T	rs9510701	0.05421
NM_014363.6(SACS):c.909A>G (p.Ala303=)	rs41315020	0.03313
NM_014363.6(SACS):c.1839G>A (p.Gln613=)	rs35840595	0.02863
NM_014363.6(SACS):c.11032C>G (p.Pro3678Ala)	rs17078601	0.02418
NM_014363.6(SACS):c.7149C>T (p.Arg2383=)	rs17078608	0.01409
NM_014363.6(SACS):c.8345C>T (p.Ala2782Val)	rs61742500	0.00776
NM_014363.6(SACS):c.8344G>A (p.Ala2782Thr)	rs61742502	0.00775
NM_014363.6(SACS):c.4188C>T (p.His1396=)	rs61754477	0.00688
NM_014363.6(SACS):c.6267G>A (p.Ser2089=)	rs9550956	0.00688
NM_014363.6(SACS):c.2983G>T (p.Val995Phe)	rs142967124	0.00134
NM_014363.6(SACS):c.*677C>T	rs200375761	0.00014
NM_000231.3(SGCG):c.*136T>C	rs3751372
NM_014363.6(SACS):c.*1046CTTTA[1]	rs66920661

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