| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9770242 | 0.851 | 0.240 | 7 | 106285885 | 5 prime UTR variant | C/A | snv | 0.79 | 5 | ||
| rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 | ||
| rs9529561 | 1.000 | 0.080 | 13 | 69325374 | downstream gene variant | A/G | snv | 6.3E-02 | 1 | ||
| rs945177 | 1.000 | 0.080 | 13 | 27047848 | intergenic variant | G/A;T | snv | 1 | |||
| rs909253 | 0.641 | 0.600 | 6 | 31572536 | intron variant | A/G;T | snv | 34 | |||
| rs885479 | 0.732 | 0.280 | 16 | 89919746 | missense variant | G/A | snv | 0.15 | 8.3E-02 | 16 | |
| rs867186 | 0.752 | 0.120 | 20 | 35176751 | missense variant | A/G | snv | 0.10 | 9.7E-02 | 15 | |
| rs842647 | 0.827 | 0.400 | 2 | 60892336 | intron variant | G/A | snv | 0.62 | 6 | ||
| rs8177375 | 0.925 | 0.080 | 11 | 126293169 | 3 prime UTR variant | A/G | snv | 0.12 | 0.13 | 2 | |
| rs8177374 | 0.672 | 0.520 | 11 | 126292948 | missense variant | C/T | snv | 0.12 | 0.11 | 22 | |
| rs805305 | 0.882 | 0.120 | 6 | 31729610 | intron variant | C/G | snv | 0.48 | 3 | ||
| rs77874543 | 0.882 | 0.080 | 22 | 41926712 | missense variant | G/C;T | snv | 6.1E-02 | 5.5E-02 | 3 | |
| rs773829498 | 0.882 | 0.080 | 7 | 101130457 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
| rs773520745 | 0.882 | 0.120 | 19 | 18075817 | missense variant | C/G;T | snv | 2.0E-05; 4.0E-06 | 3 | ||
| rs747126003 | 0.689 | 0.400 | 7 | 22728790 | missense variant | A/G;T | snv | 4.0E-06 | 18 | ||
| rs7119750 | 0.882 | 0.120 | 11 | 65655120 | 3 prime UTR variant | C/G;T | snv | 3 | |||
| rs7096206 | 0.708 | 0.480 | 10 | 52771925 | upstream gene variant | G/A;C;T | snv | 17 | |||
| rs7022797 | 0.882 | 0.120 | 9 | 88989548 | upstream gene variant | T/G | snv | 0.38 | 3 | ||
| rs6958571 | 0.925 | 0.080 | 7 | 30446094 | intron variant | A/C;G | snv | 1.2E-05; 0.25; 5.3E-05 | 3 | ||
| rs6586282 | 0.882 | 0.080 | 21 | 43058387 | intron variant | C/T | snv | 5 | |||
| rs653765 | 0.763 | 0.240 | 15 | 58749813 | upstream gene variant | T/C;G | snv | 0.45 | 10 | ||
| rs61330082 | 0.732 | 0.320 | 7 | 106286419 | upstream gene variant | G/A | snv | 0.22 | 13 | ||
| rs595209 | 0.925 | 0.080 | 11 | 126292326 | intron variant | A/C;G | snv | 2 | |||
| rs58764888 | 1.000 | 0.080 | 3 | 11176005 | intron variant | T/A | snv | 5.8E-02 | 1 |