List of variants reported as uncertain significance for Spinocerebellar ataxia type 5 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006946.4(SPTBN2):c.6953C>T (p.Ser2318Leu)	rs780506142	0.00003
NM_006946.4(SPTBN2):c.1844G>A (p.Arg615Gln)	rs768742849	0.00002
NM_006946.4(SPTBN2):c.542C>A (p.Ala181Asp)
NM_006946.4(SPTBN2):c.571G>T (p.Ala191Ser)	rs2496527683
NM_006946.4(SPTBN2):c.6373G>C (p.Gly2125Arg)

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