| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs608114 | 0.925 | 6 | 95928822 | intron variant | A/T | snv | 0.95 | 5 | |||
| rs10831234 | 1.000 | 11 | 94500021 | downstream gene variant | C/T | snv | 0.11 | 1 | |||
| rs73132848 | 0.882 | 0.080 | 3 | 8764738 | intron variant | G/A | snv | 9.3E-02 | 6 | ||
| rs12460243 | 0.925 | 19 | 8066356 | intron variant | G/A | snv | 0.14 | 5 | |||
| rs17169 | 0.925 | 2 | 8037334 | intron variant | G/T | snv | 0.13 | 5 | |||
| rs30388 | 0.925 | 16 | 79580219 | regulatory region variant | T/C;G | snv | 5 | ||||
| rs35467001 | 0.882 | 0.080 | 17 | 73383923 | missense variant | G/A | snv | 5.3E-02 | 6.3E-02 | 6 | |
| rs6723162 | 0.925 | 2 | 70875156 | intergenic variant | A/T | snv | 0.65 | 5 | |||
| rs10808739 | 0.882 | 8 | 64727703 | intron variant | G/A | snv | 0.24 | 6 | |||
| rs6996198 | 1.000 | 8 | 64550885 | downstream gene variant | C/T | snv | 0.18 | 1 | |||
| rs1047552 | 0.925 | 0.080 | 15 | 63305658 | missense variant | T/A;G | snv | 6.1E-02 | 4.7E-02 | 2 | |
| rs11231017 | 0.925 | 11 | 62293877 | downstream gene variant | G/A | snv | 0.29 | 5 | |||
| rs146215995 | 1.000 | 11 | 5679850 | missense variant | C/A;T | snv | 8.0E-06; 9.5E-05 | 1 | |||
| rs11038628 | 1.000 | 11 | 5667710 | missense variant | C/T | snv | 0.14 | 0.14 | 1 | ||
| rs1800451 | 0.776 | 0.240 | 10 | 52771466 | missense variant | C/T | snv | 3.2E-02 | 7.9E-02 | 9 | |
| rs1544410 | 0.542 | 0.760 | 12 | 47846052 | intron variant | C/A;G;T | snv | 78 | |||
| rs17878969 | 1.000 | 12 | 47842624 | 3 prime UTR variant | TTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT | delins | 1 | ||||
| rs1126477 | 0.807 | 0.200 | 3 | 46459778 | missense variant | C/T | snv | 0.34 | 0.53 | 7 | |
| rs1126478 | 0.763 | 0.240 | 3 | 46459723 | missense variant | T/C | snv | 0.41 | 0.51 | 11 | |
| rs1015164 | 0.925 | 3 | 46410189 | intron variant | A/C;G;T | snv | 8 | ||||
| rs147879075 | 1.000 | 3 | 46373902 | stop gained | C/A;G;T | snv | 1.6E-05; 8.2E-06; 4.1E-06 | 1 | |||
| rs184279915 | 1.000 | 3 | 46373708 | missense variant | G/A;T | snv | 3.2E-05; 1.2E-05 | 1 | |||
| rs541069027 | 1.000 | 3 | 46373290 | missense variant | G/A | snv | 1.8E-04 | 4.2E-05 | 1 | ||
| rs183662584 | 1.000 | 3 | 46373218 | missense variant | G/A | snv | 5.2E-04 | 1.5E-04 | 2 | ||
| rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 68 |