Gene entry
CYP1A2
cytochrome P450 family 1 subfamily A member 2
- Chromosome
- 15
- Cytoband
- 15q24.1
- Variants (rsID)
- 40
CYP1A2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q24.1). Its official name is “cytochrome P450 family 1 subfamily A member 2”. The reference table lists 40 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs2470890Benignsynonymous_variantPure Autonomic Failure|Breast Cancer|Mental Depression|Major Depressive Disorder|Depression|Hemosiderosis|Rare Hereditary Hemochromatosis|Glioma Susceptibility 1|Tardive Dyskinesia|Neutropenia|Schizophrenia|Type 2 Diabetes Mellitus|Microvascular Complications of Diabetes 5|Diabetes Mellitus|High-Grade Astrocytoma
- rs762551Likely benignsingle nucleotide variant
Other listed variants
- rs2069522
- rs2069525
- rs2069526
- rs2472304
- rs3743484
- rs4646425
- rs4646427
- rs4646428
- rs12592480
- rs12720461
- rs17861152
- rs28399417
- rs28399418
- rs28399424
- rs34067076
- rs34151816
- rs35796837
- rs45442197
- rs45468096
- rs45486893
- rs45540640
- rs45565238
- rs55889066
- rs56107638
- rs56160784
- rs56276455
- rs60086777
- rs72547512
- rs72547515
- rs72547517
- rs138652540
- rs144148965
- rs149928755
- rs183165301
- rs192799115
- rs201485133
- rs202191520
- rs374094758
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.