| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800872 | 0.495 | 0.840 | 1 | 206773062 | 5 prime UTR variant | T/G | snv | 0.69 | 119 | ||
| rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
| rs1800871 | 0.508 | 0.800 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 0.69 | 108 | ||
| rs5275 | 0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv | 55 | |||
| rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 40 | ||
| rs3021097 | 0.752 | 0.440 | 1 | 206773289 | 5 prime UTR variant | A/G | snv | 10 | |||
| rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 9 | |||
| rs6790 | 0.790 | 0.320 | 1 | 173865494 | non coding transcript exon variant | G/A | snv | 8.9E-02 | 7 | ||
| rs7538876 | 0.807 | 0.120 | 1 | 17395867 | intron variant | G/A | snv | 0.37 | 6 | ||
| rs3126085 | 0.851 | 0.280 | 1 | 152328341 | intron variant | G/A | snv | 0.29 | 5 | ||
| rs3813946 | 0.827 | 0.280 | 1 | 207454348 | 5 prime UTR variant | T/C | snv | 0.16 | 5 | ||
| rs801114 | 0.827 | 0.120 | 1 | 228862088 | downstream gene variant | T/G | snv | 0.48 | 5 | ||
| rs3790844 | 0.882 | 0.200 | 1 | 200038304 | intron variant | A/C;G | snv | 4 | |||
| rs1373589952 | 1.000 | 0.120 | 1 | 206772296 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs2275531 | 1.000 | 0.120 | 1 | 206935771 | missense variant | C/G;T | snv | 0.38 | 1 | ||
| rs291102 | 1.000 | 0.120 | 1 | 206933133 | missense variant | G/A;C | snv | 0.10 | 1 | ||
| rs3783553 | 0.667 | 0.480 | 2 | 112774138 | 3 prime UTR variant | -/TGAA | delins | 26 | |||
| rs13387042 | 0.732 | 0.280 | 2 | 217041109 | intergenic variant | A/G | snv | 0.44 | 16 | ||
| rs12621278 | 0.790 | 0.280 | 2 | 172446825 | intron variant | A/G | snv | 4.9E-02 | 7 | ||
| rs13397985 | 0.827 | 0.280 | 2 | 230226508 | intron variant | T/C;G | snv | 5 | |||
| rs17483466 | 0.827 | 0.280 | 2 | 111039881 | intron variant | A/G | snv | 0.15 | 5 | ||
| rs6435862 | 0.827 | 0.160 | 2 | 214807822 | intron variant | G/A;C;T | snv | 5 | |||
| rs721048 | 0.851 | 0.200 | 2 | 62904596 | intron variant | G/A | snv | 0.13 | 4 | ||
| rs757978 | 0.851 | 0.200 | 2 | 241431686 | missense variant | C/A;T | snv | 4.1E-06; 9.3E-02 | 4 | ||
| rs1465618 | 0.882 | 0.160 | 2 | 43326810 | intron variant | T/C | snv | 0.80 | 3 |