rs139224520 SMUG1P1 - ACAA2
T allele associated with decreased risk of Phospholipids to Total Lipids in Very Large HDL percentage (OR=0.21). [GWAS Catalog]
What is rs139224520?
rs139224520 is a single-nucleotide polymorphism (SNP) in the SMUG1P1 - ACAA2 gene. Each person carries two copies, one from each parent, so a result is reported as a pair of letters such as TT. The table below describes what studies associate with each genotype; the association is statistical, across populations, and is not a diagnosis.
What does each rs139224520 genotype mean?
| Genotype | Association | What the evidence says | Confidence |
|---|---|---|---|
| TT | typical / lower | T allele associated with decreased risk of Phospholipids to Total Lipids in Very Large HDL percentage (OR=0.21). [GWAS Catalog] | 90% |
Is rs139224520 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
- PubMed 41044249
- GWAS Catalog
- GCST90500458
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What is my genotype at rs139224520 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.