"GeneDx"[submitter] AND "CYP1A2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151221	GRCh38/hg38 15q24.1(chr15:74724230-74756760)x1	CYP1A1, CYP1A2 +2 more	Copy number loss	See cases	GLikely benign
Select item 511079	NM_000761.5(CYP1A2):c.-9-154C>A	CYP1A2, LOC110467516	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 675798	NM_000761.5(CYP1A2):c.1548= (p.Asn516=)	CYP1A2	Variation (no sequence alteration)	not provided	GBenign
Select item 254015	GRCh37/hg19 15q24.1-24.3(chr15:74368270-78122737)x3	ARID3B, C15orf39 +49 more	Copy number gain	See cases	GUncertain significance
Select item 253605	GRCh37/hg19 15q24.1-24.2(chr15:72998989-76069787)x3	ADPGK, ARID3B +47 more	Copy number gain	See cases	GPathogenic
Select item 253560	GRCh37/hg19 15q24.1-24.2(chr15:72958539-75569605)x1	ADPGK, ARID3B +37 more	Copy number loss	See cases	GPathogenic
Select item 253516	GRCh37/hg19 15q22.31-26.3(chr15:64637227-102509910)x3	AAGAB, ABHD17C +278 more	Copy number gain	See cases	GPathogenic

ClinVar