Variant (rsID / SNP)
rs2470890
rs2470890 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP1A2. Location: chromosome 15, position 75,047,426. Clinical significance in the table: Benign.
Reference-table entries
CYP1A2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- synonymous_variant
- Chromosome / position
- 15:75047426
- HGVS
- NM_000761.5,c.1548C>T,p.Asn516Asn
- Allele change
- Synonymous_N516N
Associated conditions / phenotypes
Pure 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
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.