Variant (rsID / SNP)

rs405509

rs405509 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOE. Location: chromosome 19, position 45,408,836. Clinical significance in the table: risk factor.

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Reference-table entries

APOERisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 19:45408836
Cytoband: 19q13.32
HGVS: NM_000041.2(APOE):c.-286T=

Associated conditions / phenotypes

Coronary artery disease, severe, susceptibility to

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.