| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
| rs781230344 | 1.000 | 0.080 | 8 | 104014559 | missense variant | C/G | snv | 4.8E-05 | 2 | ||
| rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 39 | |
| rs1801673 | 0.882 | 0.120 | 11 | 108304736 | missense variant | A/T | snv | 4.9E-03 | 4.4E-03 | 3 | |
| rs3802842 | 0.695 | 0.280 | 11 | 111300984 | intron variant | C/A | snv | 0.71 | 25 | ||
| rs462779 | 0.851 | 0.120 | 6 | 111374684 | missense variant | G/A | snv | 0.72 | 0.67 | 4 | |
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
| rs2705535 | 1.000 | 0.080 | 3 | 112490080 | intron variant | C/T | snv | 8.4E-02 | 1 | ||
| rs776197565 | 0.827 | 0.120 | 5 | 112819214 | missense variant | G/C;T | snv | 4.0E-06; 4.0E-06 | 5 | ||
| rs1143623 | 0.677 | 0.440 | 2 | 112838252 | upstream gene variant | C/G | snv | 0.24 | 29 | ||
| rs11536898 | 0.882 | 0.080 | 9 | 117717932 | 3 prime UTR variant | C/A | snv | 0.14 | 3 | ||
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs3753584 | 0.827 | 0.080 | 1 | 11804529 | 5 prime UTR variant | T/C | snv | 0.14 | 10 | ||
| rs1061624 | 0.776 | 0.320 | 1 | 12207208 | 3 prime UTR variant | A/G | snv | 0.48 | 8 | ||
| rs1800449 | 0.641 | 0.400 | 5 | 122077513 | missense variant | C/A;T | snv | 4.0E-06; 0.17 | 33 | ||
| rs1801726 | 0.732 | 0.280 | 3 | 122284985 | missense variant | G/C | snv | 0.95 | 0.92 | 13 | |
| rs1525489 | 1.000 | 0.080 | 7 | 122993419 | downstream gene variant | A/G | snv | 3.6E-02 | 1 | ||
| rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
| rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 | |||
| rs9637365 | 1.000 | 0.080 | 3 | 126651323 | intron variant | T/C | snv | 0.48 | 1 | ||
| rs11718498 | 1.000 | 0.080 | 3 | 126654076 | intron variant | G/A | snv | 0.36 | 1 | ||
| rs2632159 | 0.882 | 0.080 | 8 | 127021159 | intron variant | G/A;T | snv | 3 | |||
| rs6983267 | 0.578 | 0.440 | 8 | 127401060 | non coding transcript exon variant | G/T | snv | 0.37 | 62 | ||
| rs2853668 | 0.882 | 0.080 | 5 | 1299910 | upstream gene variant | G/T | snv | 0.33 | 5 |