Variant (rsID / SNP)
rs8192719
rs8192719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2B6. Location: chromosome 19, position 41,518,773. The table records no clinical significance for this variant.
Reference-table entries
CYP2B6Not classified
- Variant type
- intron_variant
- Chromosome / position
- 19:41518773
- HGVS
- NM_000767.5,c.1294+53C>T
- Allele change
- Silent
Associated conditions / phenotypes
Ischemia|Efavirenz, Poor Metabolism of
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.