Traits - Triglyceride levels
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Triglycerides are the main type of fat in blood and food. They store and transport energy and are part of the standard lipid panel.
GWAS work has identified many variants influencing triglyceride levels, including those in APOA5, LPL, and ANGPTL3.
This result reflects research-level variation in triglyceride biology and is not a lipid panel or treatment plan.
Recent meals, alcohol, weight, activity, blood sugar, and medications strongly affect actual triglyceride values.
Average genetic tendency
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Review the genes, tested markers and supporting research.
These are the unique genetic markers analyzed for this trait. Genotypes showing "--" were not identified in your DNA file. Report marker totals can include repeated study entries; this table shows each SNP once.
| SNP | Chromosome | Genotype | Variant allele | Frequency |
|---|---|---|---|---|
| rs2289123 | TT | T | 31.00% | |
| rs114606502 | -- | C | 0.10% | |
| rs114699399 | -- | A | 1.00% | |
| rs11665759 | -- | G | 5.00% | |
| rs1260326 | -- | 40.00% | ||
| rs138142645 | -- | G | 2.00% | |
| rs142551805 | -- | A | 4.00% | |
| rs143008449 | -- | A | 2.00% | |
| rs150310295 | -- | T | 2.00% | |
| rs184753612 | -- | A | 2.00% | |
| rs4522365 | -- | T | 17.00% | |
| rs4665972 | -- | C | 40.00% | |
| rs549237563 | -- | G | 1.00% | |
| rs551107164 | -- | G | 1.00% | |
| rs568152609 | -- | C | 1.00% | |
| rs59778223 | -- | A | 3.00% | |
| rs73123056 | -- | A | 4.00% | |
| rs75219957 | -- | G | 2.00% | |
| rs78637841 | -- | G | 0.96% | |
| rs9836545 | -- | C | 2.00% | |
| rs114536492 | -- | T | 2.00% | |
| rs116102213 | -- | G | 5.00% | |
| rs12128312 | -- | A | 4.00% | |
| rs138087311 | -- | C | 2.00% | |
| rs139243855 | -- | C | 1.00% | |
| rs146746145 | -- | G | 2.00% | |
| rs147513759 | -- | C | 1.00% | |
| rs56043653 | -- | A | 1.00% | |
| rs62243377 | -- | C | 1.00% | |
| rs72950184 | -- | C | 1.00% | |
| rs72966461 | -- | T | 1.00% | |
| rs76529322 | -- | T | 3.00% | |
| rs7922453 | -- | T | 1.00% |
DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence (build 37/HG19). Other companies may use the opposite strand, so genotypes may need conversion for comparison.
The following peer-reviewed scientific studies support the genetic associations analyzed in this report.
Authors: Wan JY, Goodman DL, Willems EL, Freedland AR, Norden-Krichmar TM, Santorico SA, Edwards KL,
Study sample: 516 individuals (european ancestry)
