Genetic Predisposition

Based on your genetic markers, your predisposition to this trait is shown below

Your Result

Higher Worry susceptibility predisposition

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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
rs1938386 1 GT T 56.93%
rs17196295 2 GG G 10.40%
rs9829032 3 GG G 38.10%
rs1248860 3 AA A 55.27%
rs353547 3 CC C 65.32%
rs9870384 3 CT T 22.98%
rs10005233 4 CT T 66.81%
rs1593304 7 GG G 59.42%
rs1163085 10 AA A 63.90%
rs3740688 11 GT T 63.92%
rs3026401 11 CT T 64.32%
rs4752856 11 GA A 25.72%
rs4245150 11 TT T 80.39%
rs10501320 11 GC C 8.83%
rs1017730 11 AA A 16.99%
rs10769256 11 CT T 35.96%
rs10850379 12 CT T 34.11%
rs888415 14 GG G 54.23%
rs9671386 14 AA A 73.32%
rs7152906 14 TC C 34.19%
rs722599 14 TC C 41.43%
rs10871777 18 AG G 24.58%
rs1539844 18 GA A 8.65%
rs9966951 18 GA A 32.71%
rs2488401 1 -- T 23.64%
rs488359 1 -- G 57.65%
rs61731122 1 -- A 0.90%
rs1296171 1 -- G 55.85%
rs12145083 1 -- A 16.21%
rs34644694 1 -- A 70.09%
rs2710323 -- C 52.18%
rs332828 1 -- A 35.46%
rs79827531 2 -- A 12.16%
rs2672852 2 -- T 54.39%
rs998884 2 -- G 38.98%
rs78260322 2 -- G 3.17%
rs7567451 2 -- T 56.67%
rs730356 2 -- A 12.20%
rs76508707 3 -- T 45.33%
rs4684833 3 -- T 79.69%
rs9811546 3 -- A 22.78%
rs9828595 3 -- G 23.04%
rs2236939 3 -- T 11.16%
rs4687552 3 -- C 30.97%
rs818219 3 -- C 58.71%
rs62253085 3 -- G 54.57%
rs62250661 3 -- A 40.83%
rs7355953 3 -- C 10.00%
rs480330 3 -- T 41.95%
rs13094915 3 -- A 44.95%
rs61734645 3 -- G 1.96%
rs525773 3 -- A 56.09%
rs589092 3 -- G 47.90%
rs4856278 3 -- G 83.25%
rs34135146 3 -- C 4.53%
rs9836178 3 -- C 72.70%
rs9837462 3 -- A 15.81%
rs9854869 3 -- A 11.22%
rs1368748 3 -- G 49.60%
rs9861237 3 -- C 34.86%
rs4434138 3 -- G 34.13%
rs4405857 3 -- C 60.64%
rs352140 3 -- T 41.55%
rs6445541 3 -- T 33.75%
rs1724725 3 -- G 97.96%
rs6807666 3 -- C 64.52%
rs13324323 3 -- T 22.78%
rs57360718 4 -- C 8.03%
rs10034259 4 -- C 14.32%
rs6851494 4 -- C 68.65%
rs502652 5 -- T 19.73%
rs16902946 5 -- C 0.00%
rs2194027 5 -- A 31.89%
rs12188167 5 -- G 6.77%
rs391236 5 -- G 19.29%
rs246914 5 -- C 12.46%
rs13328187 5 -- C 14.48%
rs1572982 6 -- A 59.07%
rs3117425 6 -- T 4.45%
rs483143 6 -- C 12.60%
rs34569203 6 -- C 9.66%
rs13262595 8 -- G 75.96%
rs13282237 8 -- G 60.22%
rs2407746 8 -- G 22.56%
rs28639817 8 -- G 15.24%
rs150491901 8 -- A 4.87%
rs4526367 8 -- A 78.19%
rs17532098 9 -- T 5.03%
rs75614054 9 -- T 5.15%
rs62551581 9 -- C 8.89%
rs7023933 9 -- T 28.85%
rs7033345 9 -- C 38.66%
rs6478623 9 -- G 36.14%
rs3740393 10 -- C 21.03%
rs3740397 10 -- C 35.02%
rs77420391 10 -- A 15.16%
rs12260436 10 -- C 35.54%
rs11191392 10 -- A 51.46%
rs12765002 10 -- T 28.17%
rs1890184 10 -- C 42.31%
rs1826787 10 -- T 22.98%
rs4937872 11 -- G 60.94%
rs56133711 11 -- A 11.34%
rs3742020 12 -- C 33.65%
rs10507274 12 -- C 2.42%
rs1426371 12 -- A 25.66%
rs3124377 13 -- T 59.88%
rs1330745 13 -- C 11.00%
rs61991614 14 -- A 14.24%
rs3213716 14 -- A 31.15%
rs11159097 14 -- C 31.67%
rs28426374 14 -- T 52.38%
rs9936170 16 -- G 45.55%
rs59735493 16 -- A 43.55%
rs3751855 16 -- C 47.96%
rs12923795 16 -- C 30.73%
rs55997507 16 -- C 57.47%
rs11204421 17 -- C 38.76%
rs7207400 17 -- C 26.30%
rs7220839 17 -- T 41.05%
rs3785879 17 -- A 46.77%
rs2435210 17 -- T 25.14%
rs62064641 17 -- C 8.69%
rs12938031 17 -- G 17.07%
rs60642411 17 -- A 24.94%
rs3988211 17 -- G 97.18%
rs8067056 17 -- C 30.91%
rs75195552 17 -- A 9.01%
rs56084168 17 -- T 16.49%
rs9896243 17 -- G 12.32%
rs11663050 18 -- G 45.67%
rs62081537 18 -- C 17.01%
rs62096058 18 -- A 33.57%
rs62081501 18 -- A 5.41%
rs4799723 18 -- G 78.41%
rs3897644 18 -- T 50.78%
rs12957516 18 -- T 46.75%
rs72893199 18 -- C 15.81%
rs1427041 18 -- G 74.94%
rs77432625 19 -- G 5.39%
rs112591851 19 -- T 0.90%
rs1998122 20 -- A 31.09%
rs2413631 22 -- A 19.17%
rs11090045 22 -- A 21.29%
rs12484971 22 -- T 25.16%
rs34011394 22 -- T 28.85%
rs80533 22 -- G 82.59%
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: 24/147 SNPs detected (16%)
Reference: Human Genome Build 37 (HG19)
Generated: March 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.