| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs762151808 | 0.925 | 0.040 | 14 | 94378559 | missense variant | A/C | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs112434206 | 1.000 | 0.040 | 5 | 33083283 | intron variant | A/C;G | snv | 7.6E-03 | 3 | ||
| rs114821210 | 1.000 | 0.040 | 5 | 166089843 | intergenic variant | C/A | snv | 6.0E-03 | 3 | ||
| rs12362161 | 1.000 | 0.040 | 11 | 98834502 | intergenic variant | C/A;G | snv | 3 | |||
| rs139130723 | 1.000 | 0.040 | 6 | 14411553 | intergenic variant | A/G | snv | 4.4E-03 | 3 | ||
| rs142803096 | 1.000 | 0.040 | 6 | 14420151 | intergenic variant | G/C | snv | 4.4E-03 | 3 | ||
| rs144303414 | 1.000 | 0.040 | 18 | 48509413 | intergenic variant | A/C | snv | 1.5E-02 | 3 | ||
| rs148133894 | 1.000 | 0.040 | 16 | 24584678 | intergenic variant | T/C | snv | 2.4E-03 | 3 | ||
| rs188344082 | 1.000 | 0.040 | 1 | 18783262 | intergenic variant | G/A | snv | 1.8E-02 | 3 | ||
| rs541284506 | 1.000 | 0.040 | 5 | 30425422 | intergenic variant | G/A | snv | 4.4E-03 | 3 | ||
| rs61945053 | 1.000 | 0.040 | 13 | 27021678 | upstream gene variant | G/A | snv | 2.5E-02 | 3 | ||
| rs74056623 | 1.000 | 0.040 | 1 | 18784584 | intergenic variant | G/A | snv | 8.3E-02 | 3 | ||
| rs74056624 | 1.000 | 0.040 | 1 | 18790006 | intergenic variant | G/A | snv | 2.3E-02 | 3 | ||
| rs79661299 | 1.000 | 0.040 | 6 | 42088268 | downstream gene variant | C/G;T | snv | 3 | |||
| rs749303395 | 0.882 | 0.040 | 1 | 114680329 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs11110004 | 1.000 | 0.040 | 12 | 99694540 | intron variant | T/C | snv | 5.1E-03 | 3 | ||
| rs1253810269 | 0.882 | 0.080 | 1 | 26696971 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
| rs61823501 | 1.000 | 0.040 | 1 | 184396836 | intron variant | C/T | snv | 0.12 | 3 | ||
| rs16917667 | 1.000 | 0.040 | 8 | 95439600 | intron variant | G/A | snv | 4.1E-02 | 3 | ||
| rs74864598 | 1.000 | 0.040 | 8 | 95439207 | intron variant | C/A | snv | 4.4E-02 | 3 | ||
| rs149322277 | 1.000 | 0.040 | 16 | 87925065 | intron variant | C/T | snv | 5.6E-03 | 3 | ||
| rs150109621 | 1.000 | 0.040 | 22 | 46429532 | intron variant | C/T | snv | 5.9E-03 | 3 | ||
| rs150381023 | 1.000 | 0.040 | 22 | 46423108 | intron variant | T/C | snv | 5.8E-03 | 3 | ||
| rs535263906 | 1.000 | 0.040 | 22 | 46422493 | intron variant | G/A | snv | 8.6E-03 | 3 | ||
| rs10927887 | 0.925 | 0.040 | 1 | 16024780 | missense variant | A/C;G | snv | 0.55 | 3 |