Variant (rsID / SNP)

rs1799853

rs1799853 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C9. Location: chromosome 10, position 96,702,047. Clinical significance in the table: Likely benign; drug response; other.

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Reference-table entries

CYP2C9Likely benign

Clinical significance (as recorded): Likely benign; drug response; other
Variant type: single nucleotide variant
Chromosome / position: 10:96702047
Cytoband: 10q23.33
HGVS: CYP2C9*2
Allele change: Missense_R144C

Associated conditions / phenotypes

Warfarin response|Piroxicam response|Flurbiprofen response|Lesinurad response|Phenytoin 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.