List of variants in gene combination DNMT1, LOC126862853 reported as uncertain significance for autosomal dominant cerebellar ataxia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.4492G>A (p.Gly1498Ser)	rs768764350	0.00001
NM_001130823.3(DNMT1):c.4636C>G (p.Pro1546Ala)	rs1555687655
NM_001130823.3(DNMT1):c.4711C>T (p.Arg1571Cys)

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