| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 7 | ||
| rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 5 | |||
| rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 4 | ||
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
| rs121913529 | 0.492 | 0.680 | 12 | 25245350 | missense variant | C/A;G;T | snv | 4.0E-06 | 3 | ||
| rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs34424986 | 0.752 | 0.200 | 6 | 161785820 | missense variant | G/A;T | snv | 1.9E-03; 8.0E-06 | 2 | ||
| rs5030807 | 0.851 | 0.320 | 3 | 10142113 | missense variant | T/A;C | snv | 2 | |||
| rs1057519697 | 0.776 | 0.120 | 2 | 29220830 | missense variant | A/C | snv | 1 | |||
| rs1057519698 | 0.827 | 0.120 | 2 | 29222347 | missense variant | A/G;T | snv | 1 | |||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
| rs121913338 | 0.677 | 0.400 | 7 | 140753354 | missense variant | T/A;C;G | snv | 1 | |||
| rs121913469 | 0.763 | 0.240 | 17 | 39723966 | missense variant | TT/CC | mnv | 1 | |||
| rs1360631927 | 0.851 | 0.200 | 19 | 45369114 | missense variant | C/T | snv | 7.0E-06 | 1 | ||
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 1 | |
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 1 | |
| rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 1 | |||
| rs200100285 | 0.851 | 0.080 | 1 | 11796313 | missense variant | T/C;G | snv | 1.9E-04 | 1 | ||
| rs121965039 | 0.851 | 0.160 | 10 | 124408601 | missense variant | C/A;T | snv | 8.0E-06 | 1 | ||
| rs142771326 | 1.000 | 0.080 | 11 | 111766340 | missense variant | C/G;T | snv | 2.0E-04 | 5.2E-04 | 1 | |
| rs1805076 | 0.851 | 0.120 | 11 | 111764842 | missense variant | C/T | snv | 6.5E-03 | 7.0E-03 | 1 | |
| rs973682124 | 1.000 | 0.080 | 11 | 111743419 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs2241880 | 0.627 | 0.600 | 2 | 233274722 | missense variant | A/G | snv | 0.45 | 0.44 | 1 | |
| rs121917737 | 0.827 | 0.080 | 10 | 79557264 | missense variant | C/A | snv | 1 | |||
| rs121917738 | 0.827 | 0.080 | 10 | 79557363 | missense variant | A/G | snv | 1 |