Variant (rsID / SNP)

rs28399447

rs28399447 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2A6. Location: chromosome 19, position 41,352,941. Clinical significance in the table: drug response.

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Reference-table entries

CYP2A6Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 19:41352941
Cytoband: 19q13.2
HGVS: NM_000762.5(CYP2A6):c.670T>C (p.Ser224Pro)
Allele change: Missense_S224P

Associated conditions / phenotypes

Tegafur 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.