| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs149447933 | 1.000 | 0.040 | 6 | 14453908 | intron variant | C/G | snv | 4.4E-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 | ||
| rs16917667 | 1.000 | 0.040 | 8 | 95439600 | intron variant | G/A | snv | 4.1E-02 | 3 | ||
| rs1700575 | 1.000 | 0.040 | 5 | 8543925 | intron variant | A/T | snv | 0.26 | 3 | ||
| rs188344082 | 1.000 | 0.040 | 1 | 18783262 | intergenic variant | G/A | snv | 1.8E-02 | 3 | ||
| rs189919070 | 1.000 | 0.040 | 3 | 134436825 | upstream gene variant | C/A;T | snv | 3 | |||
| rs200536955 | 0.925 | 0.040 | 19 | 35756980 | missense variant | G/A;T | snv | 7.0E-04 | 3 | ||
| rs3829365 | 0.925 | 0.040 | 13 | 37598759 | 5 prime UTR variant | G/A;C | snv | 4.0E-06; 0.11 | 3 | ||
| rs535263906 | 1.000 | 0.040 | 22 | 46422493 | intron variant | G/A | snv | 8.6E-03 | 3 | ||
| rs541284506 | 1.000 | 0.040 | 5 | 30425422 | intergenic variant | G/A | snv | 4.4E-03 | 3 | ||
| rs6026584 | 0.925 | 0.040 | 20 | 58894018 | intron variant | T/C | snv | 0.70 | 3 | ||
| rs61823501 | 1.000 | 0.040 | 1 | 184396836 | intron variant | C/T | snv | 0.12 | 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 | ||
| rs74864598 | 1.000 | 0.040 | 8 | 95439207 | intron variant | C/A | snv | 4.4E-02 | 3 | ||
| rs749303395 | 0.882 | 0.040 | 1 | 114680329 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs78314028 | 1.000 | 0.040 | 7 | 6163445 | 3 prime UTR variant | C/A | snv | 2.2E-02 | 3 | ||
| rs7965830 | 1.000 | 0.040 | 12 | 75962050 | intron variant | C/A;T | snv | 3 | |||
| rs79661299 | 1.000 | 0.040 | 6 | 42088268 | downstream gene variant | C/G;T | snv | 3 | |||
| rs8105292 | 1.000 | 0.040 | 19 | 32103916 | non coding transcript exon variant | T/C | snv | 0.19 | 3 | ||
| rs9470398 | 1.000 | 0.040 | 6 | 36799290 | intron variant | T/C | snv | 5.5E-02 | 3 | ||
| rs958546 | 0.882 | 0.040 | 13 | 46259582 | intron variant | G/C | snv | 0.29 | 3 | ||
| rs10932374 | 0.925 | 0.040 | 2 | 211379678 | 3 prime UTR variant | G/A | snv | 0.23 | 2 |