rs3846662 HMGCR
Drug response
What is rs3846662?
rs3846662 is a single-nucleotide polymorphism (SNP) in the HMGCR gene. Each person carries two copies, one from each parent, so a result is reported as a pair of letters such as CT. The table below describes what studies associate with each genotype; the association is statistical, across populations, and is not a diagnosis.
What does each rs3846662 genotype mean?
| Genotype | Association | What the evidence says | Confidence |
|---|
Which drugs have annotations for rs3846662?
PharmGKB clinical annotations (level 1A is the strongest evidence, 4 the weakest):
| Drug | Annotation type | Evidence level |
|---|---|---|
| simvastatin | Other, Efficacy | 3 |
| HMG-CoA reductase inhibitors | Other, Efficacy | 3 |
Is rs3846662 on 23andMe and AncestryDNA chips?
Chip coverage is not recorded for this variant. Orviva reports it when a raw-data file contains it directly or via a well-correlated proxy SNP, and says so when it does not.
Sources
- PharmGKB:3
- Drug:simvastatin
- Type:Other
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What is my genotype at rs3846662 and what does it mean for me?”
Genetic associations describe risk across populations, not a diagnosis for any one person. Most variants shift risk modestly and act alongside lifestyle, environment and other genes. Consumer DNA chips do not read every position and can be wrong at any single one. For general education only; talk to a clinician or genetic counsellor before acting on anything here, and never change a prescribed medicine without your prescriber.