Genetic Tendency

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

Genetic Association

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Higher worry tendency

This is a weak, population-level genetic association, not a personal diagnosis or a definitive trait.

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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
rs10005233 TT 33.19%
rs1572982 AA A 59.07%
rs1593304 GG 40.58%
rs17196295 AG G 10.40%
rs353547 CC 34.68%
rs1938386 GT T 56.93%
rs9671386 GA 26.68%
rs9811546 GA A 22.78%
rs1163085 GA A 63.90%
rs1248860 GA 44.73%
rs12938031 GG G 17.07%
rs2710323 CC C 52.18%
rs3026401 CT 35.68%
rs7152906 TC 65.81%
rs722599 CC C 41.43%
rs7355953 TC C 10.00%
rs888415 GG 45.77%
rs1017730 GA A 16.99%
rs10769256 TT T 35.96%
rs10871777 AG G 24.58%
rs1539844 GA A 8.65%
rs9829032 AG G 38.10%
rs9966951 GA A 32.71%
rs3740688 TT 36.08%
rs3897644 CT 49.22%
rs9870384 CT T 22.98%
rs10034259 -- C 14.32%
rs13324323 -- T 22.78%
rs150491901 -- A 4.87%
rs28639817 -- G 15.24%
rs332828 -- A 35.46%
rs34644694 -- 29.91%
rs391236 -- G 19.29%
rs4405857 -- 39.36%
rs4684833 -- 20.31%
rs480330 -- T 41.95%
rs483143 -- C 12.60%
rs488359 -- G 57.65%
rs502652 -- T 19.73%
rs57360718 -- C 8.03%
rs61731122 -- A 0.90%
rs62253085 -- 45.43%
rs62551581 -- C 8.89%
rs7033345 -- C 38.66%
rs7567451 -- T 56.67%
rs78260322 -- G 3.17%
rs79827531 -- A 12.16%
rs998884 -- G 38.98%
rs12188167 -- G 6.77%
rs2488401 -- T 23.64%
rs2672852 -- 45.61%
rs1724725 -- 2.04%
rs17532098 -- T 5.03%
rs2236939 -- T 11.16%
rs13262595 -- 24.04%
rs2413631 -- A 19.17%
rs2435210 -- T 25.14%
rs246914 -- C 12.46%
rs11663050 -- G 45.67%
rs12145083 -- A 16.21%
rs12260436 -- C 35.54%
rs12484971 -- T 25.16%
rs12765002 -- T 28.17%
rs12923795 -- 69.27%
rs12957516 -- 53.25%
rs13094915 -- C 55.05%
rs13282237 -- G 60.22%
rs1330745 -- C 11.00%
rs13328187 -- C 14.48%
rs1368748 -- 50.40%
rs28426374 -- T 52.38%
rs3117425 -- T 4.45%
rs3124377 -- 40.12%
rs3742020 -- C 33.65%
rs3751855 -- C 47.96%
rs3988211 -- 2.82%
rs4245150 -- 19.61%
rs4752856 -- A 25.72%
rs4799723 -- 21.59%
rs4856278 -- 16.75%
rs4937872 -- G 60.94%
rs525773 -- A 56.09%
rs55997507 -- 42.53%
rs56084168 -- T 16.49%
rs56133711 -- A 11.34%
rs589092 -- 52.10%
rs59735493 -- A 43.55%
rs60642411 -- A 24.94%
rs61734645 -- G 1.96%
rs61991614 -- A 14.24%
rs62064641 -- C 8.69%
rs62081501 -- A 5.41%
rs62081537 -- C 17.01%
rs62096058 -- A 33.57%
rs62250661 -- A 40.83%
rs6445541 -- T 33.75%
rs6478623 -- G 36.14%
rs6807666 -- 35.48%
rs6851494 -- 31.35%
rs7023933 -- T 28.85%
rs7207400 -- C 26.30%
rs7220839 -- T 41.05%
rs72893199 -- C 15.81%
rs730356 -- A 12.20%
rs75195552 -- A 9.01%
rs75614054 -- T 5.15%
rs76508707 -- T 45.33%
rs77420391 -- A 15.16%
rs77432625 -- G 5.39%
rs80533 -- 17.41%
rs8067056 -- C 30.91%
rs818219 -- C 58.71%
rs9936170 -- G 45.55%
rs9861237 -- C 34.86%
rs9836178 -- 27.30%
rs10501320 -- C 8.83%
rs10507274 -- C 2.42%
rs10850379 -- T 34.11%
rs11090045 -- A 21.29%
rs11159097 -- C 31.67%
rs11191392 -- A 51.46%
rs11204421 -- C 38.76%
rs112591851 -- T 0.90%
rs1426371 -- A 25.66%
rs1427041 -- 25.06%
rs16902946 -- C 0.00%
rs1826787 -- T 22.98%
rs1890184 -- C 42.31%
rs9854869 -- A 11.22%
rs3213716 -- A 31.15%
rs34011394 -- T 28.85%
rs34135146 -- C 4.53%
rs34569203 -- C 9.66%
rs352140 -- 58.45%
rs3740393 -- C 21.03%
rs3740397 -- C 35.02%
rs3785879 -- A 46.77%
rs4434138 -- G 34.13%
rs4526367 -- 21.81%
rs4687552 -- C 30.97%
rs2194027 -- A 31.89%
rs1998122 -- A 31.09%
rs9896243 -- G 12.32%
rs1296171 -- G 55.85%
rs2407746 -- G 22.56%
rs9837462 -- A 15.81%
rs9828595 -- G 23.04%
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: 26/147 SNPs detected (17%)
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.