| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12692386 | 0.827 | 0.160 | 2 | 9555777 | 5 prime UTR variant | A/G | snv | 0.72 | 5 | ||
| rs12191786 | 0.851 | 0.120 | 6 | 22004398 | intron variant | C/A;T | snv | 4 | |||
| rs1524668 | 0.851 | 0.160 | 2 | 9557243 | upstream gene variant | A/C | snv | 0.64 | 4 | ||
| rs2479409 | 1.000 | 0.040 | 1 | 55038977 | upstream gene variant | G/A | snv | 0.66 | 4 | ||
| rs7025486 | 0.851 | 0.040 | 9 | 121660124 | intron variant | G/A | snv | 0.28 | 4 | ||
| rs12133641 | 0.925 | 0.040 | 1 | 154455807 | intron variant | A/G | snv | 0.44 | 3 | ||
| rs12695895 | 0.925 | 0.040 | 3 | 148725481 | intron variant | C/T | snv | 0.31 | 3 | ||
| rs4916251 | 0.882 | 0.040 | 1 | 172377256 | intron variant | T/A | snv | 0.70 | 3 | ||
| rs595244 | 0.882 | 0.080 | 15 | 48548638 | intron variant | C/T | snv | 7.7E-02 | 3 | ||
| rs764522 | 0.882 | 0.080 | 3 | 30605058 | upstream gene variant | G/A;C | snv | 3 | |||
| rs7866503 | 0.882 | 0.080 | 9 | 22091925 | intron variant | G/T | snv | 0.50 | 3 | ||
| rs8003379 | 0.882 | 0.160 | 14 | 64406881 | intron variant | A/C | snv | 0.23 | 3 | ||
| rs8087799 | 0.882 | 0.080 | 18 | 22605468 | regulatory region variant | G/A | snv | 0.43 | 3 | ||
| rs919433 | 0.882 | 0.080 | 2 | 197301841 | intron variant | G/A | snv | 0.38 | 3 | ||
| rs137854485 | 0.925 | 0.160 | 15 | 48515402 | missense variant | G/A | snv | 2 | |||
| rs2234681 | 1.000 | 0.040 | 20 | 46008773 | upstream gene variant | ACACACACACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACACAC;ACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACAC;ACACACACACACACACACACACACACACACACAC | delins | 2 | |||
| rs3019885 | 0.925 | 0.120 | 8 | 117013406 | intron variant | T/A;G | snv | 2 | |||
| rs326118 | 0.925 | 0.080 | 5 | 7868430 | intron variant | T/G | snv | 0.21 | 2 | ||
| rs3827066 | 0.925 | 0.040 | 20 | 45957384 | intron variant | C/T | snv | 0.12 | 2 | ||
| rs4988300 | 0.925 | 0.120 | 11 | 68321363 | intron variant | G/T | snv | 0.50 | 2 | ||
| rs1036095 | 1.000 | 0.040 | 3 | 30620836 | intron variant | C/G | snv | 0.72 | 1 | ||
| rs1057518075 | 1.000 | 0.040 | 2 | 188995061 | stop gained | C/T | snv | 1 | |||
| rs10758278 | 1.000 | 0.040 | 9 | 34825306 | intron variant | G/A | snv | 0.53 | 1 | ||
| rs10985349 | 1.000 | 0.040 | 9 | 121662964 | intron variant | C/T | snv | 0.17 | 1 | ||
| rs13382862 | 1.000 | 0.040 | 2 | 20682689 | upstream gene variant | A/G;T | snv | 0.59 | 1 |