Genetic Tendency

Based on your genetic markers, your tendency toward this trait is shown below

Your Result

Higher life satisfaction tendency

Was this result accurate for you?

Scientific Evidence

These are the genetic markers (SNPs) analyzed for this trait. Variations detected in your genome are listed under the "Genotype" column. SNPs showing "--" were not identified in your DNA file.

SNP Chromosome Genotype Variant Allele Frequency
rs11607056 CT T 32.11%
rs2093623 AA A 48.87%
rs261940 GG G 47.29%
rs2978362 TT T 52.16%
rs4526571 GA A 38.30%
rs6869941 CT T 49.59%
rs716508 TT T 68.24%
rs7396827 TC C 53.45%
rs10252771 GG G 31.97%
rs10497655 TC C 31.09%
rs10809441 CT T 44.83%
rs1660237 CT T 42.03%
rs2715147 CT T 49.91%
rs3134012 CC C 71.92%
rs3793577 AG G 53.16%
rs6771444 GA A 50.27%
rs913021 CT T 64.04%
rs9546806 TT T 61.12%
rs10774909 -- G 20.31%
rs10783484 -- T 25.20%
rs10818400 -- G 60.57%
rs11192283 -- C 23.40%
rs1155156 -- A 60.18%
rs11693031 -- G 33.09%
rs12083196 -- C 23.08%
rs12791990 -- C 14.08%
rs12962538 -- C 18.18%
rs12967831 -- A 33.52%
rs1371325 -- G 59.70%
rs1431071 -- T 28.51%
rs1490176 -- A 71.51%
rs149979 -- A 22.98%
rs17417046 -- T 44.32%
rs1829526 -- G 19.80%
rs2015971 -- T 44.86%
rs2149351 -- G 75.89%
rs215816 -- A 29.73%
rs2398144 -- A 40.43%
rs2514226 -- C 74.69%
rs263575 -- A 45.20%
rs28687557 -- A 77.90%
rs35267052 -- G 10.66%
rs3781627 -- A 69.41%
rs57713596 -- T 12.84%
rs59925771 -- T 10.52%
rs61905363 -- T 3.89%
rs62551639 -- C 6.22%
rs6776145 -- C 12.08%
rs6896348 -- G 51.31%
rs6925748 -- G 42.05%
rs71301807 -- G 24.20%
rs7170398 -- T 39.98%
rs7191427 -- T 25.27%
rs72694240 -- G 16.13%
rs7374731 -- G 74.68%
rs77214504 -- T 4.54%
rs918814 -- C 58.56%
rs9967747 -- C 86.49%
rs10737452 -- T 62.52%
rs10765186 -- T 50.74%
rs10916951 -- T 39.35%
rs10967509 -- A 37.94%
rs111871194 -- C 9.90%
rs112028067 -- A 21.81%
rs11214441 -- A 39.59%
rs11214596 -- G 53.50%
rs114595701 -- T 9.25%
rs1150752 -- C 11.21%
rs12436091 -- C 76.00%
rs12479300 -- A 35.83%
rs12587457 -- T 50.61%
rs12794371 -- T 33.16%
rs12930743 -- C 55.15%
rs12959642 -- G 77.40%
rs12960889 -- C 56.81%
rs13198298 -- T 10.13%
rs13217239 -- C 36.45%
rs13396259 -- G 30.22%
rs1452787 -- G 28.43%
rs1460939 -- T 80.31%
rs1484680 -- G 58.25%
rs1506 -- A 80.61%
rs1518395 -- G 61.34%
rs1558804 -- G 45.10%
rs164640 -- T 52.97%
rs17041417 -- A 18.07%
rs17622606 -- A 4.66%
rs17782464 -- G 15.65%
rs1903845 -- T 35.77%
rs1964390 -- G 75.40%
rs198457 -- T 18.78%
rs2071303 -- C 34.93%
rs210915 -- T 80.50%
rs2191130 -- T 68.27%
rs2239549 -- A 37.92%
rs2290850 -- C 34.82%
rs2299502 -- C 38.77%
rs2342502 -- G 46.13%
rs2458167 -- C 68.58%
rs2690083 -- T 34.54%
rs2813608 -- A 65.45%
rs2919980 -- C 51.41%
rs297343 -- G 63.71%
rs308774 -- T 20.38%
rs3094669 -- G 13.57%
rs3115672 -- T 11.36%
rs3130614 -- A 11.92%
rs325501 -- C 57.87%
rs34020413 -- G 38.26%
rs35368417 -- C 44.04%
rs3824344 -- T 37.29%
rs4304650 -- C 80.15%
rs4461738 -- C 46.46%
rs4581549 -- T 11.72%
rs4711107 -- C 29.02%
rs4711152 -- C 45.08%
rs4799464 -- T 69.41%
rs4914984 -- G 76.95%
rs584564 -- G 91.17%
rs6019826 -- T 13.30%
rs6090940 -- T 32.26%
rs62460794 -- A 57.50%
rs62620225 -- T 3.96%
rs66530963 -- G 14.92%
rs66993685 -- A 23.08%
rs6721577 -- T 58.36%
rs6769821 -- A 73.86%
rs68006638 -- A 8.63%
rs6943746 -- G 38.57%
rs7154329 -- G 49.95%
rs7232516 -- A 13.21%
rs7243332 -- G 30.56%
rs7422667 -- C 56.37%
rs7526171 -- C 62.54%
rs7606466 -- G 56.99%
rs7766749 -- C 9.55%
rs7949802 -- T 42.80%
rs7989827 -- G 49.11%
rs8084280 -- T 50.84%
rs8089474 -- A 80.43%
rs815710 -- G 40.72%
rs876308 -- A 41.70%
rs9287989 -- C 50.66%
rs9295661 -- A 92.16%
rs9380010 -- G 25.02%
rs9393716 -- G 19.79%
rs9564496 -- A 31.84%
rs9601120 -- T 18.61%
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.

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Coverage: 18/148 SNPs detected (12%)
Reference: Human Genome Build 37 (HG19)
Generated: June 02, 2026
DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence. Other testing companies may report using the opposite strand, requiring conversion for accurate comparison.