Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs439401

APOE

rs439401 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOE. Location: chromosome 19, position 45,414,451. Clinical significance in the table: drug response.

Reference-table entries

APOEDrug response
Clinical significance (as recorded)
drug response
Variant type
single nucleotide variant
Chromosome / position
19:45414451
Cytoband
19q13.32
HGVS
NC_000019.9:g.45414451T>C

Associated conditions / phenotypes

Warfarin response

Public references

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