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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060823	NM_015698.6(GPKOW):c.1335G>A (p.Arg445=)	GPKOW	Single nucleotide variant (synonymous variant)	GPKOW-related condition	GBenign
Select item 2298895	NM_015698.6(GPKOW):c.1327C>T (p.Arg443Trp)	GPKOW (R443W)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3056587	NM_015698.6(GPKOW):c.1297-4C>T	GPKOW	Single nucleotide variant (intron variant)	GPKOW-related condition	GBenign
Select item 3061022	NM_015698.6(GPKOW):c.456+10C>T	GPKOW	Single nucleotide variant (intron variant)	GPKOW-related condition	GBenign
Select item 731666	NM_015698.6(GPKOW):c.429G>C (p.Gly143=)	GPKOW	Single nucleotide variant (synonymous variant)	GPKOW-related condition +1 more	GBenign
Select item 711049	NM_015698.6(GPKOW):c.366G>A (p.Ala122=)	GPKOW	Single nucleotide variant (synonymous variant)	GPKOW-related condition +1 more	GLikely benign
Select item 3059955	NM_015698.6(GPKOW):c.11C>G (p.Ser4Cys)	GPKOW (S4C)	Single nucleotide variant (missense variant)	GPKOW-related condition	GBenign

ClinVar