"PreventionGenetics, part of Exact Sciences"[submitter] AND "ABCG2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3041649	NM_004827.3(ABCG2):c.1582G>A (p.Ala528Thr)	ABCG2 (A526T +1 more)	Single nucleotide variant (missense variant)	ABCG2-related disorder	GLikely benign
Select item 3044880	NM_004827.3(ABCG2):c.1060G>A (p.Gly354Arg)	ABCG2 (G352R +1 more)	Single nucleotide variant (missense variant)	ABCG2-related disorder	GLikely benign
Select item 3057392	NM_004827.3(ABCG2):c.841+3A>G	ABCG2	Single nucleotide variant (intron variant)	ABCG2-related disorder	GLikely benign
Select item 30389	NM_004827.3(ABCG2):c.421C>A (p.Gln141Lys)	ABCG2 (Q141K)	Single nucleotide variant (missense variant)	rosuvastatin response - Metabolism/PK +1 more	Gdrug response
Select item 3059818	NM_004827.3(ABCG2):c.263+10A>G	ABCG2	Single nucleotide variant (intron variant)	ABCG2-related disorder	GBenign
Select item 30386	NM_004827.3(ABCG2):c.34G>A (p.Val12Met)	ABCG2 (V12M)	Single nucleotide variant (missense variant)	ABCG2-related disorder	GLikely benign

ClinVar