"GeneDx"[submitter] AND "AHR"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58518	GRCh38/hg38 7p21.3-21.1(chr7:9975653-19356878)x1	AGMO, AGR2 +130 more	Copy number loss	See cases	GPathogenic
Select item 59679	GRCh38/hg38 7p21.2-15.2(chr7:16234212-26167278)x3	ABCB5, AGR2 +287 more	Copy number gain	See cases	GPathogenic
Select item 59568	GRCh38/hg38 7p21.1(chr7:16838053-17672667)x3	AGR3, AHR +16 more	Copy number gain	See cases	GUncertain significance
Select item 151570	GRCh38/hg38 7p21.1(chr7:17238688-17474079)x3	AHR, LINC02888 +6 more	Copy number gain	See cases	GBenign
Select item 1168239	NM_001621.5(AHR):c.1661G>A (p.Arg554Lys)	AHR (R554K)	Single nucleotide variant (missense variant)	not provided	GBenign

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