| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10504062 | 8 | 47824663 | intron variant | T/C | snv | 2.1E-02 | 3 | ||||
| rs10518982 | 15 | 58507555 | intron variant | A/G | snv | 2.2E-02 | 3 | ||||
| rs10986881 | 9 | 125756807 | intron variant | C/T | snv | 1.8E-02 | 3 | ||||
| rs11193085 | 10 | 106873848 | intron variant | G/A | snv | 8.8E-02 | 3 | ||||
| rs11574728 | 7 | 80676025 | intron variant | G/A | snv | 7.5E-03 | 3 | ||||
| rs11925396 | 3 | 194391622 | downstream gene variant | A/G | snv | 1.9E-02 | 3 | ||||
| rs12708979 | 16 | 56978442 | intron variant | C/T | snv | 5.9E-03 | 3 | ||||
| rs16940391 | 15 | 58507449 | intron variant | C/A;G | snv | 3 | |||||
| rs17120434 | 11 | 117204969 | 3 prime UTR variant | A/G;T | snv | 5.4E-02 | 3 | ||||
| rs1713222 | 2 | 21048451 | upstream gene variant | A/G | snv | 0.82 | 3 | ||||
| rs34499590 | 1 | 65616108 | missense variant | C/G;T | snv | 2.5E-03 | 3 | ||||
| rs5020 | 17 | 44255219 | splice region variant | A/G | snv | 3.2E-03 | 1.3E-02 | 3 | |||
| rs5743316 | 4 | 186082537 | missense variant | A/T | snv | 4.0E-05 | 3.5E-05 | 3 | |||
| rs7100433 | 10 | 133370298 | intron variant | T/C | snv | 0.98 | 3 | ||||
| rs7827408 | 8 | 99527615 | intron variant | C/T | snv | 2.3E-02 | 3 | ||||
| rs7951347 | 11 | 19198031 | intron variant | T/A;C | snv | 3 | |||||
| rs876528 | 5 | 159964639 | intron variant | G/A | snv | 2.3E-02 | 3 | ||||
| rs9658150 | 6 | 35420123 | splice region variant | G/A | snv | 3.6E-05 | 5.6E-05 | 3 | |||
| rs9658465 | 12 | 117247093 | intron variant | T/G | snv | 2.3E-02 | 3 | ||||
| rs9658736 | 10 | 89004160 | intron variant | T/C | snv | 9.4E-03 | 3 | ||||
| rs9838771 | 3 | 30657290 | intron variant | G/A | snv | 2.5E-02 | 3 | ||||
| rs9912177 | 17 | 47285851 | intron variant | A/T | snv | 6.4E-03 | 3 | ||||
| rs10156121 | 7 | 142672656 | downstream gene variant | T/C | snv | 3.9E-02 | 4 | ||||
| rs10415849 | 19 | 19394278 | intron variant | C/T | snv | 0.12 | 4 | ||||
| rs10500212 | 19 | 19612406 | intron variant | C/T | snv | 0.10 | 4 |