| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10162249 | 1.000 | 0.040 | 13 | 25849519 | intron variant | T/C | snv | 0.14 | 1 | ||
| rs10467674 | 1.000 | 0.040 | 13 | 25854100 | intron variant | T/A | snv | 0.14 | 1 | ||
| rs10484399 | 0.851 | 0.240 | 6 | 27566749 | intergenic variant | A/G | snv | 5.4E-02 | 3 | ||
| rs1049550 | 0.882 | 0.160 | 10 | 80166946 | missense variant | G/A;C | snv | 0.42; 4.2E-06 | 1 | ||
| rs10741657 | 0.637 | 0.520 | 11 | 14893332 | upstream gene variant | A/G | snv | 0.65 | 1 | ||
| rs111877852 | 1.000 | 0.040 | 6 | 32378632 | intron variant | AGATAGAT/-;AGAT;AGATAGATAGAT;AGATAGATAGATAGAT;AGATAGATAGATAGATAGAT;AGATAGATAGATAGATAGATAGAT;AGATAGATAGATAGATAGATAGATAGAT | delins | 3.3E-02 | 1 | ||
| rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
| rs112198380 | 1.000 | 0.040 | 13 | 25855238 | intron variant | A/G | snv | 0.14 | 1 | ||
| rs11244 | 0.925 | 0.160 | 6 | 32812947 | 3 prime UTR variant | G/A | snv | 0.27 | 1 | ||
| rs112668322 | 1.000 | 0.040 | 6 | 33606422 | intergenic variant | G/A;T | snv | 1 | |||
| rs113520250 | 1.000 | 0.040 | 6 | 32587108 | intron variant | C/T | snv | 0.26 | 1 | ||
| rs113585425 | 1.000 | 0.040 | 6 | 32465348 | intron variant | A/C | snv | 7.8E-02 | 1 | ||
| rs113653545 | 1.000 | 0.040 | 6 | 32482426 | intergenic variant | C/T | snv | 8.9E-02 | 1 | ||
| rs114060570 | 1.000 | 0.040 | 6 | 32485791 | intergenic variant | C/T | snv | 9.9E-02 | 1 | ||
| rs114480004 | 1.000 | 0.040 | 6 | 32623583 | upstream gene variant | G/C | snv | 4.8E-02 | 1 | ||
| rs114549185 | 1.000 | 0.040 | 6 | 32633427 | intron variant | C/G | snv | 5.2E-02 | 1 | ||
| rs11465804 | 0.752 | 0.320 | 1 | 67236843 | intron variant | T/G | snv | 4.4E-02 | 5.4E-02 | 3 | |
| rs114798579 | 1.000 | 0.040 | 6 | 32629564 | intron variant | G/A | snv | 4.6E-02 | 1 | ||
| rs114812135 | 1.000 | 0.040 | 6 | 32619184 | intergenic variant | A/T | snv | 4.7E-02 | 1 | ||
| rs115080784 | 1.000 | 0.040 | 6 | 32457111 | downstream gene variant | C/T | snv | 4.7E-02 | 1 | ||
| rs115673262 | 1.000 | 0.040 | 6 | 32604965 | intergenic variant | C/G | snv | 1 | |||
| rs115736757 | 1.000 | 0.040 | 6 | 32607947 | intergenic variant | T/C | snv | 4.7E-02 | 1 | ||
| rs116119619 | 1.000 | 0.040 | 6 | 32607948 | intergenic variant | G/A | snv | 4.7E-02 | 1 | ||
| rs12020004 | 1.000 | 0.040 | 13 | 25851513 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs12194148 | 0.925 | 0.160 | 6 | 32476421 | upstream gene variant | G/C;T | snv | 2 |