| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4784677 | 1.000 | 0.120 | 16 | 56514589 | missense variant | C/T | snv | 0.99 | 1.00 | 1 | |
| rs4302331 | 1.000 | 0.120 | 3 | 33014229 | missense variant | A/G | snv | 0.98 | 0.93 | 1 | |
| rs820878 | 1.000 | 0.120 | 5 | 74685445 | missense variant | T/C | snv | 0.97 | 0.97 | 1 | |
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 4 | |
| rs450046 | 0.851 | 0.280 | 22 | 18913491 | missense variant | C/T | snv | 0.93 | 2.8E-03 | 2 | |
| rs12021720 | 0.925 | 0.160 | 1 | 100206504 | missense variant | T/A;C | snv | 0.92 | 1 | ||
| rs3826549 | 1.000 | 0.080 | 17 | 41586466 | missense variant | A/G;T | snv | 0.64 | 1 | ||
| rs3733402 | 1.000 | 0.040 | 4 | 186236880 | missense variant | G/A;C | snv | 0.54 | 1 | ||
| rs2071460 | 1.000 | 0.080 | 11 | 11352722 | missense variant | A/G | snv | 0.48 | 0.41 | 1 | |
| rs2241880 | 0.627 | 0.600 | 2 | 233274722 | missense variant | A/G | snv | 0.45 | 0.44 | 1 | |
| rs25640 | 5 | 119475838 | missense variant | G/A;C | snv | 0.45 | 1 | ||||
| rs2236225 | 0.614 | 0.640 | 14 | 64442127 | missense variant | G/A | snv | 0.44 | 0.38 | 1 | |
| rs61749665 | 1.000 | 0.040 | 17 | 8003201 | missense variant | G/T | snv | 0.42 | 0.30 | 1 | |
| rs12150220 | 0.724 | 0.360 | 17 | 5582047 | missense variant | A/T | snv | 0.37 | 0.33 | 1 | |
| rs6504649 | 0.882 | 0.280 | 17 | 50360095 | missense variant | C/G;T | snv | 0.33; 3.2E-05 | 1 | ||
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 1 | |
| rs1008642 | 0.882 | 0.120 | 3 | 8733975 | missense variant | C/A;G;T | snv | 0.29 | 1 | ||
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
| rs6688832 | 0.752 | 0.440 | 1 | 9263851 | missense variant | G/A;C | snv | 0.28; 1.2E-04 | 1 | ||
| rs2301600 | 0.925 | 0.040 | 19 | 35295965 | missense variant | C/G;T | snv | 0.27 | 1 | ||
| rs4792311 | 0.776 | 0.160 | 17 | 13011692 | missense variant | G/A;C | snv | 0.27 | 1 | ||
| rs28564871 | 1.000 | 0.080 | 14 | 50901892 | missense variant | A/G;T | snv | 0.24; 4.2E-06 | 1 | ||
| rs6811423 | 1.000 | 0.080 | 4 | 3492873 | missense variant | A/G | snv | 0.23 | 0.18 | 1 | |
| rs3829868 | 0.925 | 0.080 | 1 | 152409644 | missense variant | C/T | snv | 0.21 | 0.15 | 1 | |
| rs1064039 | 0.827 | 0.200 | 20 | 23637790 | missense variant | C/G;T | snv | 0.20 | 1 |