Variant (rsID / SNP)

rs28371685

rs28371685 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C9. Location: chromosome 10, position 96,740,981. Clinical significance in the table: Benign/Likely benign; drug response.

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Reference-table entries

CYP2C9Benign

Clinical significance (as recorded): Benign/Likely benign; drug response
Variant type: single nucleotide variant
Chromosome / position: 10:96740981
Cytoband: 10q23.33
HGVS: CYP2C9*11
Allele change: Missense_R335W

Associated conditions / phenotypes

Piroxicam response|Flurbiprofen response|Lesinurad response

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.