| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1048155 | 1.000 | 0.040 | 12 | 26120155 | 3 prime UTR variant | C/G | snv | 0.48 | 1 | ||
| rs1056562 | 1.000 | 0.040 | 11 | 118254910 | 3 prime UTR variant | T/C | snv | 0.57 | 1 | ||
| rs1057519782 | 1.000 | 0.040 | 2 | 29220734 | missense variant | G/T | snv | 1 | |||
| rs1057520012 | 1.000 | 0.040 | 4 | 65404419 | missense variant | C/T | snv | 1 | |||
| rs1057520017 | 1.000 | 0.040 | 19 | 1220630 | missense variant | C/T | snv | 1 | |||
| rs10758203 | 1.000 | 0.040 | 9 | 33421422 | intergenic variant | G/A;C | snv | 1 | |||
| rs10842496 | 1.000 | 0.040 | 12 | 25158555 | missense variant | G/A;T | snv | 2.8E-04; 0.33 | 1 | ||
| rs11048413 | 1.000 | 0.040 | 12 | 26122622 | missense variant | G/A | snv | 0.53 | 0.38 | 1 | |
| rs114807680 | 1.000 | 0.040 | 3 | 135085649 | intron variant | G/A | snv | 9.8E-03 | 1 | ||
| rs114928225 | 1.000 | 0.040 | 2 | 118692164 | intergenic variant | T/A | snv | 1.0E-02 | 1 | ||
| rs116080888 | 1.000 | 0.040 | 6 | 32618459 | intergenic variant | C/A | snv | 1 | |||
| rs11632038 | 1.000 | 0.040 | 15 | 49314101 | intron variant | A/G | snv | 0.15 | 1 | ||
| rs116506680 | 1.000 | 0.040 | 6 | 29813272 | upstream gene variant | T/A;C;G | snv | 1 | |||
| rs117151283 | 1.000 | 0.040 | 13 | 45539328 | intron variant | C/G;T | snv | 1 | |||
| rs1171516758 | 1.000 | 0.040 | 7 | 55142377 | synonymous variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs117634027 | 1.000 | 0.040 | 10 | 88340394 | intron variant | G/T | snv | 2.6E-03 | 1 | ||
| rs11855650 | 1.000 | 0.040 | 15 | 70139434 | intergenic variant | G/T | snv | 0.39 | 1 | ||
| rs1193127627 | 1.000 | 0.040 | 9 | 74842272 | missense variant | C/A | snv | 4.0E-06 | 1 | ||
| rs1216460058 | 1.000 | 0.040 | 7 | 6046097 | missense variant | C/T | snv | 1 | |||
| rs12503223 | 1.000 | 0.040 | 4 | 16841093 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs1388363572 | 1.000 | 0.040 | 15 | 88135386 | missense variant | C/A | snv | 7.0E-06 | 1 | ||
| rs1390558952 | 1.000 | 0.040 | 6 | 149683082 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs140361050 | 1.000 | 0.040 | 16 | 48230493 | synonymous variant | C/T | snv | 2.3E-04; 4.0E-06 | 2.3E-04 | 1 | |
| rs1403821912 | 1.000 | 0.040 | 8 | 26864422 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1423790481 | 1.000 | 0.040 | 9 | 22008805 | missense variant | G/A | snv | 4.5E-06 | 1 |