Variant (rsID / SNP)
rs186335453
rs186335453 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2B6. Location: chromosome 19, position 41,510,063. 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
- 19:41510063
- Cytoband
- 19q13.2
- HGVS
- NM_000767.5(CYP2B6):c.329G>T (p.Gly110Val)
- Allele change
- Missense_G110V
Associated conditions / phenotypes
Efavirenz response
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.