Variant (rsID / SNP)

rs7412

rs7412 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOE. Location: chromosome 19, position 45,412,079. Clinical significance in the table: drug response.

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Reference-table entries

APOEDrug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 19:45412079
Cytoband: 19q13.32
HGVS: NM_000041.2(APOE):c.526C>T (p.Arg176Cys)
Allele change: Missense_R176C

Associated conditions / phenotypes

Familial type 3 hyperlipoproteinemia|atorvastatin response - Efficacy|Warfarin response|Hypercholesterolemia

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.