Related gene-specific medical variations for Gene (Select 1544) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340913	GRCh37/hg19 15q24.1(chr15:75047425-75073422)x1	CYP1A2	Copy number loss	not provided	GUncertain significance
Select item 1340749	GRCh37/hg19 15q24.1(chr15:75022462-75042747)x1	CYP1A2	Copy number loss	not provided	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

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