List of variants reported as uncertain significance for cerebellar degeneration by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_014363.6(SACS):c.1373C>T (p.Thr458Ile)	rs61729954	0.00227
NM_033064.5(ATCAY):c.442G>A (p.Ala148Thr)	rs200021943	0.00021
NM_000051.4(ATM):c.7475T>G (p.Leu2492Arg)	rs56399857	0.00019
NM_000051.4(ATM):c.8156G>A (p.Arg2719His)	rs55982963	0.00015
NM_002739.5(PRKCG):c.1747G>A (p.Val583Met)	rs143513754	0.00014
NM_000051.4(ATM):c.902G>A (p.Gly301Asp)	rs202208861	0.00007
NM_002739.5(PRKCG):c.715C>T (p.Arg239Trp)	rs1471641294

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