| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 14 | ||
| rs34612342 | 0.653 | 0.400 | 1 | 45332803 | missense variant | T/C | snv | 1.5E-03 | 1.6E-03 | 11 | |
| rs36053993 | 0.677 | 0.280 | 1 | 45331556 | missense variant | C/T | snv | 3.0E-03 | 3.3E-03 | 9 | |
| rs12075 | 0.724 | 0.240 | 1 | 159205564 | missense variant | G/A | snv | 0.51 | 0.66 | 8 | |
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 8 | ||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 6 | |
| rs4245739 | 0.708 | 0.360 | 1 | 204549714 | 3 prime UTR variant | C/A;G | snv | 0.77; 6.2E-06 | 6 | ||
| rs2235544 | 0.742 | 0.240 | 1 | 53909897 | intron variant | C/A;T | snv | 0.53; 4.0E-06 | 4 | ||
| rs301806 | 0.851 | 0.120 | 1 | 8422018 | intron variant | C/T | snv | 0.62 | 4 | ||
| rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 4 | |
| rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 3 | |||
| rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 2 | ||
| rs11552449 | 0.925 | 0.080 | 1 | 113905767 | missense variant | C/G;T | snv | 0.22 | 0.15 | 2 | |
| rs121908690 | 0.925 | 0.080 | 1 | 46267540 | missense variant | G/A | snv | 1.4E-05 | 2 | ||
| rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 2 | ||
| rs397514606 | 0.763 | 0.320 | 1 | 243695714 | missense variant | C/T | snv | 2 | |||
| rs4342822 | 0.882 | 0.080 | 1 | 213850882 | intron variant | G/T | snv | 0.62 | 2 | ||
| rs616488 | 0.925 | 0.080 | 1 | 10506158 | intron variant | A/G | snv | 0.27 | 2 | ||
| rs6678914 | 0.882 | 0.080 | 1 | 202218048 | intron variant | G/A | snv | 0.37 | 2 | ||
| rs750592289 | 0.925 | 0.160 | 1 | 45332786 | missense variant | G/A | snv | 8.0E-06 | 2 | ||
| rs875989854 | 0.925 | 0.160 | 1 | 75734798 | missense variant | C/G;T | snv | 8.0E-06 | 2 | ||
| rs9651118 | 0.683 | 0.480 | 1 | 11802157 | intron variant | T/C | snv | 0.18 | 2 | ||
| rs1034429230 | 1.000 | 0.080 | 1 | 212365260 | missense variant | C/G | snv | 1.4E-05 | 1 | ||
| rs112523432 | 1.000 | 0.080 | 1 | 214384776 | missense variant | T/C;G | snv | 4.0E-06; 5.9E-03 | 1 | ||
| rs1165078436 | 1.000 | 0.080 | 1 | 31798459 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 |