"PreventionGenetics, part of Exact Sciences"[submitter] AND "UGP2"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059622	NM_006759.4(UGP2):c.576-5dup	UGP2	Duplication (intron variant)	UGP2-related disorder	GLikely benign
Select item 3054653	NM_006759.4(UGP2):c.785A>G (p.Tyr262Cys)	UGP2 (Y142C +2 more)	Single nucleotide variant (missense variant)	UGP2-related disorder	GLikely benign
Select item 3054084	NM_006759.4(UGP2):c.1299C>T (p.Gly433=)	UGP2	Single nucleotide variant (synonymous variant)	UGP2-related disorder	GLikely benign

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