"CDC6-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2177973	NM_001254.4(CDC6):c.246G>A (p.Glu82=)	CDC6	Single nucleotide variant (synonymous variant)	CDC6-related condition +1 more	GLikely benign
Select item 210620	NM_001254.4(CDC6):c.640C>T (p.Arg214Trp)	CDC6 (R214W)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 323058	NM_001254.4(CDC6):c.1020G>A (p.Leu340=)	CDC6	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity

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