Variant (rsID / SNP)
rs762551
rs762551 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP1A2. Location: chromosome 15, position 75,041,917. Clinical significance in the table: Likely benign.
Reference-table entries
CYP1A2Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:75041917
- Cytoband
- 15q24.1
- HGVS
- NM_000761.5(CYP1A2):c.-9-154C>A
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.