| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 7 | ||
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 5 | |
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 4 | |
| rs6136 | 0.752 | 0.440 | 1 | 169594713 | missense variant | T/G | snv | 8.2E-02 | 7.5E-02 | 3 | |
| rs1018827 | 1 | 169544768 | intron variant | A/G | snv | 0.92 | 1 | ||||
| rs10746487 | 1 | 9278630 | intergenic variant | T/A;C | snv | 1 | |||||
| rs10919507 | 1 | 170885468 | intron variant | C/T | snv | 3.0E-02 | 1 | ||||
| rs113976843 | 1 | 170254627 | intron variant | T/C | snv | 8.6E-03 | 1 | ||||
| rs115063924 | 1 | 168741790 | intron variant | C/A;T | snv | 6.7E-03 | 1 | ||||
| rs12061601 | 1.000 | 0.040 | 1 | 169101212 | intron variant | T/C | snv | 0.16 | 1 | ||
| rs1209731 | 1 | 169355555 | intron variant | T/C;G | snv | 1 | |||||
| rs12120558 | 1 | 170366687 | downstream gene variant | G/A | snv | 1.2E-02 | 1 | ||||
| rs12122803 | 1 | 169825364 | intron variant | A/G | snv | 1.4E-02 | 1 | ||||
| rs12136148 | 1 | 170123530 | intergenic variant | T/G | snv | 6.9E-02 | 1 | ||||
| rs12732487 | 1 | 114120337 | intron variant | G/A | snv | 0.11 | 1 | ||||
| rs144405847 | 1 | 82342193 | intron variant | C/T | snv | 4.9E-02 | 1 | ||||
| rs145163454 | 1 | 169121510 | intron variant | T/C | snv | 1.6E-02 | 1 | ||||
| rs145470028 | 1 | 230850661 | intron variant | G/T | snv | 1.4E-02 | 1 | ||||
| rs16861990 | 1 | 169165889 | intron variant | A/C | snv | 5.5E-02 | 1 | ||||
| rs185120584 | 1 | 169689987 | intron variant | C/T | snv | 7.6E-03 | 1 | ||||
| rs191436110 | 1 | 170621629 | intron variant | A/G | snv | 3.0E-03 | 1 | ||||
| rs2040445 | 1 | 169247174 | intron variant | C/G;T | snv | 1 | |||||
| rs2842700 | 1 | 207108804 | intron variant | C/A;G | snv | 0.12 | 1 | ||||
| rs4524 | 1 | 169542517 | missense variant | T/C | snv | 0.28 | 0.24 | 1 | |||
| rs530059570 | 1 | 206173141 | downstream gene variant | G/A | snv | 6.2E-03 | 1 |