Genetic Predisposition

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

Your Result

Higher Calcium Levels

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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
rs6667260 1 AC C 45.79%
rs629301 1 TT T 77.80%
rs1848837 1 AG G 28.81%
rs4506486 1 CT T 60.19%
rs13389219 2 TT T 39.28%
rs780094 2 CC C 69.83%
rs1550532 2 CG G 77.96%
rs1260326 2 CC C 60.51%
rs12485738 3 GG G 62.90%
rs3773912 3 CT T 46.30%
rs9388399 6 TC C 31.13%
rs34372369 7 GA A 5.17%
rs3857708 7 AA A 29.98%
rs5745687 7 CT T 6.61%
rs1262217 10 GA A 82.56%
rs3011642 10 CT T 24.22%
rs2419886 10 CT T 25.55%
rs2377965 10 TG G 52.84%
rs10491003 10 CT T 10.40%
rs561830 11 CT T 25.18%
rs7481584 11 GA A 37.02%
rs6580981 12 GA A 45.84%
rs12369443 12 GG G 19.90%
rs7144433 14 TT T 89.23%
rs1858800 16 CT T 34.53%
rs11078597 17 TC C 18.64%
rs9910998 17 CA A 7.20%
rs7248167 19 AC C 21.70%
rs1570669 20 GG G 47.38%
rs1497826 1 -- G 37.36%
chr12:90166745 -- G 77.39%
chr20:33404922 -- T 18.66%
chr1:112218092 -- T 16.24%
chr1:150878099 -- T 22.02%
chr1:178502207 -- G 34.34%
chr5:131121243 -- C 86.69%
chr7:150502468 -- A 11.06%
chr19:50049641 -- G 25.06%
chr9:140358581 -- T 7.52%
chr11:3006027 -- A 30.54%
chr1:91544957 -- A 13.89%
chr4:75945702 -- T 6.54%
chr6:26025437 -- A 56.75%
chr7:92258733 -- A 26.71%
chr17:6614859 -- T 13.98%
chr10:9329035 -- A 32.59%
chr2:9032564 -- C 2.19%
rs3011 1 -- C 36.89%
rs760077 1 -- T 60.11%
rs841572 1 -- A 40.69%
rs1184556173 1 -- G 72.64%
rs111745074 1 -- T 21.05%
rs112174050 1 -- T 2.50%
rs148756772 1 -- C 3.23%
rs12132412 1 -- G 39.06%
rs1434282 1 -- T 72.50%
rs10737767 1 -- C 41.61%
rs61766352 1 -- C 27.87%
chr12:110749537 -- T 34.92%
rs36086195 1 -- T 57.91%
rs6576983 2 -- G 39.19%
rs7559013 2 -- C 12.95%
rs60624480 2 -- A 35.96%
rs838717 2 -- A 56.67%
rs547408441 2 -- A 4.36%
rs34636567 2 -- T 52.24%
rs111712978 2 -- A 4.74%
rs6545412 2 -- T 15.38%
rs148785604 2 -- T 56.20%
rs12467820 2 -- T 49.36%
rs12468920 2 -- G 30.70%
rs12613807 2 -- C 44.49%
rs1448208 2 -- T 33.58%
rs11673819 2 -- T 70.35%
rs10193807 2 -- C 84.02%
rs895418 2 -- T 46.93%
rs10647217 2 -- T 61.38%
rs10197122 2 -- T 7.21%
rs35154162 3 -- T 76.95%
rs16853573 3 -- C 7.67%
rs28519617 3 -- G 27.03%
rs11709284 3 -- A 55.51%
rs2593813 3 -- A 63.42%
rs13322435 3 -- G 40.39%
rs73186030 3 -- T 86.96%
rs1801725 3 -- T 9.42%
rs1801282 3 -- G 11.97%
rs531500623 3 -- A 32.62%
rs2271494 3 -- T 41.64%
rs2388993 4 -- G 58.69%
rs6841258 4 -- T 16.78%
rs13108218 4 -- G 61.57%
rs13111128 4 -- A 30.31%
rs13107325 4 -- T 7.58%
rs372867519 4 -- D 27.22%
rs7688574 4 -- T 37.07%
rs2713844 4 -- A 76.32%
rs4320103 4 -- G 3.90%
rs4864709 4 -- C 37.11%
rs6556313 5 -- G 33.18%
rs6897362 5 -- A 52.61%
rs12519940 5 -- T 27.85%
rs35841312 5 -- G 31.89%
rs251391 5 -- T 74.53%
rs10942734 5 -- C 42.84%
rs1763519 6 -- C 60.65%
rs71548342 6 -- G 17.43%
rs4946137 6 -- A 40.15%
rs7742369 6 -- G 17.48%
rs7756870 6 -- G 68.86%
rs1214761 6 -- G 67.87%
rs2327774 6 -- C 37.92%
rs4263551 6 -- C 51.65%
rs7786368 7 -- C 41.69%
rs2283038 7 -- T 23.67%
rs511220 7 -- A 40.81%
rs4718271 7 -- C 45.02%
rs3133528 8 -- C 18.10%
rs6983263 8 -- C 47.44%
rs6993770 8 -- T 28.71%
rs111291669 8 -- T 30.44%
rs28601761 8 -- G 41.90%
rs9657190 8 -- G 24.64%
rs74677734 8 -- A 4.89%
rs62493995 8 -- G 28.76%
rs62522556 8 -- C 39.87%
rs36104352 8 -- C 12.05%
rs4240624 8 -- A 90.94%
rs13283282 9 -- G 14.60%
rs11144001 9 -- T 47.15%
rs77798356 9 -- G 12.17%
rs148349564 9 -- C 8.04%
rs4740965 9 -- A 76.68%
rs4744854 9 -- C 62.73%
rs12337706 9 -- G 6.09%
rs10819178 9 -- G 63.78%
rs9411378 9 -- A 22.20%
rs546082321 10 -- C 40.09%
rs5786388 10 -- C 57.80%
rs498490 10 -- T 16.61%
rs2296436 10 -- C 8.46%
rs2274224 10 -- C 43.46%
rs9420589 10 -- T 43.45%
rs373709809 11 -- G 33.55%
rs7947953 11 -- G 61.23%
rs7928577 11 -- T 7.38%
rs302650 11 -- A 43.29%
rs36225067 11 -- C 2.62%
rs11218721 11 -- A 38.94%
rs11511848 11 -- T 62.61%
rs12363232 11 -- T 34.91%
rs2855799 11 -- A 81.16%
rs7115200 11 -- G 43.84%
rs2298615 11 -- T 23.24%
rs11172256 12 -- G 25.58%
rs199785243 12 -- C 32.51%
rs4763297 12 -- C 43.23%
rs117213754 12 -- A 1.47%
rs12320328 12 -- G 8.46%
rs17884869 12 -- A 2.46%
rs79295634 12 -- G 6.78%
rs78844280 13 -- A 2.21%
rs12583851 13 -- C 75.03%
rs7319447 13 -- G 15.13%
rs7336933 13 -- A 12.48%
rs573849602 13 -- G 26.34%
rs75153054 14 -- C 24.74%
rs35852840 14 -- A 5.80%
rs28929474 14 -- T 1.97%
rs17127600 14 -- G 17.10%
rs8011945 14 -- G 90.93%
rs11625026 14 -- T 33.09%
rs17718872 14 -- T 14.45%
rs35056049 15 -- C 71.33%
rs11071896 15 -- G 25.00%
rs147233090 15 -- T 2.48%
rs34066945 15 -- T 35.80%
rs55754498 15 -- T 5.32%
rs11629876 15 -- T 33.10%
rs11632520 15 -- T 16.92%
rs12911748 15 -- T 52.21%
rs12148513 15 -- T 37.92%
rs12918968 16 -- C 43.84%
rs16945716 16 -- C 4.90%
rs34422500 16 -- T 13.04%
rs41278174 16 -- A 2.74%
rs35610022 16 -- T 52.06%
rs2745205 16 -- G 69.81%
rs12922549 16 -- T 23.78%
rs36030405 17 -- A 23.49%
rs66634575 17 -- T 18.31%
rs77542162 17 -- G 2.27%
rs7221118 17 -- C 21.42%
rs12600694 17 -- A 19.98%
rs10852764 17 -- C 90.34%
rs5033 17 -- T 69.99%
rs2270114 17 -- C 73.36%
rs55722786 18 -- T 28.47%
rs689049 18 -- C 58.11%
rs12983362 19 -- G 26.47%
rs142888784 19 -- G 2.26%
rs143333049 19 -- G 4.02%
rs1672991 19 -- G 93.36%
rs190424317 19 -- G 13.68%
rs7252372 19 -- C 44.29%
rs73036517 19 -- G 25.96%
rs3091842 20 -- A 4.42%
rs35870583 20 -- G 18.73%
rs3787267 20 -- T 65.32%
rs73078112 20 -- T 2.72%
rs185799410 20 -- T 2.60%
rs928760 21 -- T 30.27%
rs219781 21 -- T 26.32%
rs28908470 22 -- T 32.32%
rs5760495 22 -- T 35.66%
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: 29/215 SNPs detected (13%)
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.