| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10069690 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 19 | ||
| rs1011970 | 0.677 | 0.320 | 9 | 22062135 | intron variant | G/T | snv | 0.23 | 18 | ||
| rs10146997 | 0.827 | 0.240 | 14 | 79478819 | intron variant | A/G | snv | 0.25 | 2 | ||
| rs1016604233 | 1.000 | 0.080 | 7 | 139911241 | missense variant | C/T | snv | 8.0E-06 | 2.1E-05 | 1 | |
| rs1017226 | 0.925 | 0.080 | 5 | 56857565 | intron variant | T/C | snv | 5.8E-02 | 1 | ||
| rs10235235 | 0.925 | 0.080 | 7 | 99478208 | intron variant | T/C | snv | 0.13 | 1 | ||
| rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 4 | ||
| rs10273424 | 0.925 | 0.080 | 7 | 99598450 | intron variant | T/A | snv | 0.13 | 1 | ||
| rs1033602309 | 1.000 | 0.080 | X | 9937279 | missense variant | G/C | snv | 1 | |||
| rs1034429230 | 1.000 | 0.080 | 1 | 212365260 | missense variant | C/G | snv | 1.4E-05 | 1 | ||
| rs1038304 | 0.882 | 0.160 | 6 | 151612040 | intron variant | A/G | snv | 0.58 | 1 | ||
| rs10402468 | 1.000 | 0.080 | 19 | 17273194 | intron variant | C/A | snv | 0.16 | 1 | ||
| rs10406920 | 1.000 | 0.080 | 19 | 17278839 | splice region variant | C/T | snv | 0.15 | 0.18 | 1 | |
| rs10415471 | 1.000 | 0.080 | 19 | 17250255 | synonymous variant | C/A;G;T | snv | 4.1E-06; 0.16 | 1 | ||
| rs10416654 | 1.000 | 0.080 | 19 | 17274367 | intron variant | T/C | snv | 0.17 | 1 | ||
| rs10418154 | 1.000 | 0.080 | 19 | 17275197 | intron variant | A/G | snv | 0.18 | 1 | ||
| rs10418362 | 1.000 | 0.080 | 19 | 17275298 | intron variant | A/T | snv | 0.18 | 1 | ||
| rs10419397 | 1.000 | 0.080 | 19 | 17280519 | intron variant | G/A;T | snv | 1 | |||
| rs10419742 | 1.000 | 0.080 | 19 | 17242176 | intron variant | G/C | snv | 0.11 | 1 | ||
| rs1041981 | 0.667 | 0.520 | 6 | 31573007 | missense variant | C/A | snv | 0.35 | 0.38 | 3 | |
| rs1042031 | 0.790 | 0.200 | 2 | 21002881 | stop gained | C/A;T | snv | 8.0E-06; 0.15 | 3 | ||
| rs10420922 | 1.000 | 0.080 | 19 | 17271696 | intron variant | A/T | snv | 0.42 | 0.50 | 1 | |
| rs10421287 | 1.000 | 0.080 | 19 | 17242152 | intron variant | C/T | snv | 0.11 | 1 | ||
| rs10423120 | 1.000 | 0.080 | 19 | 17311227 | intron variant | A/G | snv | 0.17 | 1 | ||
| rs10424178 | 1.000 | 0.080 | 19 | 17268749 | splice region variant | C/T | snv | 0.17 | 0.23 | 1 |