Variant (rsID / SNP)
rs1057910
rs1057910 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C9. Location: chromosome 10, position 96,741,053. Clinical significance in the table: drug response; other.
Reference-table entries
CYP2C9Drug response
- Clinical significance (as recorded)
- drug response; other
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:96741053
- Cytoband
- 10q23.33
- HGVS
- CYP2C9*3
- Allele change
- Missense_I359L
Associated conditions / phenotypes
Warfarin response|Phenytoin response|Glipizide response|Tolbutamide response|Lesinurad response|Flurbiprofen response|Piroxicam response
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.