| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10034922 | 4 | 154599476 | downstream gene variant | G/A | snv | 5.2E-02 | 3 | ||||
| rs10157379 | 1 | 247442297 | intron variant | C/G;T | snv | 3 | |||||
| rs1016988 | 5 | 132408882 | upstream gene variant | T/C | snv | 0.20 | 3 | ||||
| rs10226084 | 7 | 17957989 | upstream gene variant | T/C | snv | 0.46 | 3 | ||||
| rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 8 | |
| rs10512597 | 17 | 74703694 | intron variant | T/A;C | snv | 3 | |||||
| rs11242111 | 5 | 132420366 | intron variant | A/G;T | snv | 3 | |||||
| rs1154988 | 3 | 136206349 | upstream gene variant | T/A | snv | 0.76 | 3 | ||||
| rs12239046 | 1 | 247438293 | intron variant | T/C | snv | 0.58 | 4 | ||||
| rs12511469 | 4 | 154530607 | downstream gene variant | T/A | snv | 0.18 | 3 | ||||
| rs12651106 | 4 | 154379907 | intron variant | C/A | snv | 0.12 | 3 | ||||
| rs12712127 | 2 | 102110201 | intron variant | A/G | snv | 0.62 | 3 | ||||
| rs12777 | 5 | 132335969 | synonymous variant | C/G | snv | 3.1E-02 | 2.8E-02 | 3 | |||
| rs12915708 | 15 | 50756405 | intron variant | G/A;C | snv | 3 | |||||
| rs1476698 | 2 | 241357034 | intron variant | A/G;T | snv | 3 | |||||
| rs1539019 | 0.882 | 0.240 | 1 | 247436999 | intron variant | A/C | snv | 0.63 | 3 | ||
| rs16844401 | 1.000 | 0.040 | 4 | 3447925 | missense variant | G/A;T | snv | 7.5E-02; 8.3E-06 | 3 | ||
| rs17690122 | 5 | 132532143 | intron variant | A/G;T | snv | 3 | |||||
| rs1800787 | 1.000 | 0.040 | 4 | 154562863 | upstream gene variant | C/T | snv | 0.17 | 3 | ||
| rs1800788 | 4 | 154562762 | upstream gene variant | C/T | snv | 0.18 | 3 | ||||
| rs1800789 | 1.000 | 0.040 | 4 | 154561591 | upstream gene variant | G/A | snv | 0.17 | 3 | ||
| rs1800790 | 0.851 | 0.200 | 4 | 154562556 | upstream gene variant | G/A | snv | 0.15 | 3 | ||
| rs1938492 | 1 | 65652146 | intergenic variant | A/C | snv | 0.43 | 3 | ||||
| rs2059503 | 4 | 154572267 | downstream gene variant | A/T | snv | 0.14 | 3 | ||||
| rs2066861 | 4 | 154606284 | intron variant | C/T | snv | 0.26 | 5 |