List of variants reported as uncertain significance for Autosomal dominant cerebellar ataxia, deafness and narcolepsy

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.3353A>G (p.His1118Arg)	rs150331990	0.00002
NM_001130823.3(DNMT1):c.4492G>A (p.Gly1498Ser)	rs768764350	0.00001
NM_001130823.3(DNMT1):c.2920C>T (p.Arg974Cys)	rs2089651800
NM_001130823.3(DNMT1):c.3042G>C (p.Glu1014Asp)	rs745780816
NM_001130823.3(DNMT1):c.3311C>T (p.Ala1104Val)	rs2089593597
NM_001130823.3(DNMT1):c.4711C>T (p.Arg1571Cys)
NM_001130823.3(DNMT1):c.616G>A (p.Asp206Asn)
NM_001130823.3(DNMT1):c.650A>G (p.Asp217Gly)	rs1568249130

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