Related gene-specific medical variations for Gene (Select 196) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3102093	NM_001621.5(AHR):c.19A>G (p.Asn7Asp)	AHR, LOC129998012 (N7D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1572685	NM_001621.5(AHR):c.51G>A (p.Lys17=)	AHR, LOC129998012	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1499316	NM_001621.5(AHR):c.20A>G (p.Asn7Ser)	AHR, LOC129998012 (N7S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1489685	NM_001621.5(AHR):c.38G>T (p.Arg13Leu)	AHR, LOC129998012 (R13L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1371787	NM_001621.5(AHR):c.35G>A (p.Ser12Asn)	AHR, LOC129998012 (S12N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 226185	GRCh37/hg19 7p21.1(chr7:17243791-17590700)	AHR	Copy number gain	Abnormal esophagus morphology	GBenign

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