"PreventionGenetics, part of Exact Sciences"[submitter] AND "PGAP2"[ge - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040676	NM_014489.4(PGAP2):c.349-959A>C	PGAP2	Single nucleotide variant (synonymous variant +3 more)	PGAP2-related condition	GLikely benign
Select item 3046288	NM_014489.4(PGAP2):c.645C>G (p.Leu215=)	PGAP2 (R108G +3 more)	Single nucleotide variant (synonymous variant +2 more)	PGAP2-related condition	GLikely benign