Genetic Tendency

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

Your Result

Higher life satisfaction tendency

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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
rs10818400 GG G 60.57%
rs11607056 CT T 32.11%
rs12791990 TC C 14.08%
rs2398144 CA A 40.43%
rs2978362 CT T 52.16%
rs4526571 GA A 38.30%
rs6925748 GG G 42.05%
rs716508 TT T 68.24%
rs7396827 CC C 53.45%
rs3134012 CC C 71.92%
rs3793577 AG G 53.16%
rs6771444 AA A 50.27%
rs815710 AG G 40.72%
rs913021 TT T 64.04%
rs9287989 TC C 50.66%
rs9546806 CT T 61.12%
rs10252771 TG G 31.97%
rs10809441 CT T 44.83%
rs1660237 CT T 42.03%
rs17041417 GA A 18.07%
rs1903845 CT T 35.77%
rs2071303 TC C 34.93%
rs2715147 CT T 49.91%
rs10774909 -- G 20.31%
rs10783484 -- T 25.20%
rs11192283 -- C 23.40%
rs1155156 -- A 60.18%
rs11693031 -- G 33.09%
rs12083196 -- C 23.08%
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%
rs2093623 -- A 48.87%
rs2149351 -- G 75.89%
rs215816 -- A 29.73%
rs2514226 -- C 74.69%
rs261940 -- G 47.29%
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%
rs6869941 -- T 49.59%
rs6896348 -- G 51.31%
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%
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%
rs876308 -- A 41.70%
rs9295661 -- A 92.16%
rs9380010 -- G 25.02%
rs9393716 -- G 19.79%
rs9564496 -- A 31.84%
rs9601120 -- T 18.61%
rs10497655 -- C 31.09%
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%
rs17622606 -- A 4.66%
rs17782464 -- G 15.65%
rs1964390 -- G 75.40%
rs198457 -- T 18.78%
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%
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: 23/148 SNPs detected (15%)
Reference: Human Genome Build 37 (HG19)
Generated: October 14, 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.