Variant (rsID / SNP)
rs1208
rs1208 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAT2. Location: chromosome 8, position 18,258,316. Clinical significance in the table: drug response.
Reference-table entries
NAT2Drug response
- Clinical significance (as recorded)
- drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:18258316
- Cytoband
- 8p22
- HGVS
- NM_000015.3(NAT2):c.803= (p.Arg268=)
- Allele change
- Missense_R268K
Associated conditions / phenotypes
Slow acetylator due to N-acetyltransferase enzyme variant
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
