List of variants reported as uncertain significance for Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits by New York Genome Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_018896.5(CACNA1G):c.6958G>T (p.Gly2320Cys)	rs760308715	0.00014
NM_018896.5(CACNA1G):c.6656C>T (p.Thr2219Met)	rs1433017716	0.00002
NM_018896.5(CACNA1G):c.6769C>T (p.Arg2257Trp)	rs1444290546	0.00001
NM_018896.5(CACNA1G):c.5906T>C (p.Leu1969Pro)	rs1312607495

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