Variant (rsID / SNP)
rs28399499
rs28399499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2B6. Location: chromosome 19, position 41,518,221. Clinical significance in the table: drug response.
Reference-table entries
CYP2B6Drug response
- Clinical significance (as recorded)
- drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:41518221
- Cytoband
- 19q13.2
- HGVS
- NM_000767.5(CYP2B6):c.983T>C (p.Ile328Thr)
- Allele change
- Missense_I328T
Associated conditions / phenotypes
nevirapine response - Toxicity
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.