Variant (rsID / SNP)

rs1288601658

rs1288601658 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2C19. Location: chromosome 10, position 96,534,942. Clinical significance in the table: drug response.

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Reference-table entries

CYP2C19Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 10:96534942
Cytoband: 10q23.33
HGVS: NM_000769.4(CYP2C19):c.296A>G (p.His99Arg)
Allele change: Missense_H99R

Associated conditions / phenotypes

CYP2C19: uncertain 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.