List of variants reported as likely benign for cerebellar disorder by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001163809.2(WDR81):c.2254C>T (p.Pro752Ser)	rs200781463	0.00113
NM_001128164.2(ATXN1):c.621G>T (p.Gln207His)	rs201030692	0.00057
NM_015046.7(SETX):c.3057TGA[7] (p.Asp1024dup)	rs572772837
NM_018896.5(CACNA1G):c.5695GACAGCCCC[1] (p.1899DSP[1])	rs751210873

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