Variant (rsID / SNP)

rs118203759

rs118203759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C19. Location: chromosome 10, position 96,612,542. Clinical significance in the table: drug response.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CYP2C19Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 10:96612542
Cytoband: 10q23.33
HGVS: NM_000769.4(CYP2C19):c.1344C>G (p.Phe448Leu)
Allele change: Missense_F448L

Associated conditions / phenotypes

CYP2C19: decreased function

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.