| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs363504 | 0.882 | 0.160 | 21 | 29553607 | stop gained | A/G;T | snv | 6.7E-02 | 3 | ||
| rs363538 | 0.882 | 0.160 | 21 | 29689750 | synonymous variant | T/A;G | snv | 0.20 | 3 | ||
| rs5349 | 0.882 | 0.160 | 13 | 77903530 | synonymous variant | G/A | snv | 5.5E-03 | 1.1E-02 | 3 | |
| rs749628781 | 0.882 | 0.160 | 3 | 9934538 | missense variant | C/T | snv | 4.0E-06 | 3 | ||
| rs769233111 | 0.882 | 0.160 | 5 | 173235071 | missense variant | G/A | snv | 6.7E-05 | 2.1E-05 | 3 | |
| rs771748290 | 0.882 | 0.160 | 21 | 43072114 | missense variant | C/A;T | snv | 8.1E-06; 8.1E-06 | 3 | ||
| rs779011920 | 0.882 | 0.160 | 21 | 43066299 | missense variant | C/T | snv | 8.0E-06 | 3 | ||
| rs9024 | 0.882 | 0.160 | 21 | 36073015 | 3 prime UTR variant | G/A | snv | 9.7E-02 | 3 | ||
| rs2071421 | 0.790 | 0.200 | 22 | 50625988 | missense variant | T/C | snv | 0.17 | 0.19 | 7 | |
| rs711 | 0.851 | 0.200 | 21 | 38823135 | 3 prime UTR variant | A/C;G | snv | 4 | |||
| rs762403278 | 0.851 | 0.200 | 1 | 11796244 | missense variant | T/C;G | snv | 1.6E-05; 4.0E-06 | 4 | ||
| rs2435357 | 0.790 | 0.240 | 10 | 43086608 | intron variant | T/C | snv | 0.79 | 8 | ||
| rs12676 | 0.827 | 0.240 | 3 | 53823776 | missense variant | A/C;T | snv | 0.77 | 5 | ||
| rs1465444723 | 0.827 | 0.240 | 22 | 30610886 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
| rs28936670 | 0.708 | 0.280 | 5 | 173235011 | missense variant | G/A | snv | 3.4E-03 | 1.1E-02 | 17 | |
| rs1532268 | 0.776 | 0.280 | 5 | 7878066 | missense variant | C/T | snv | 0.31 | 0.32 | 12 | |
| rs562625029 | 0.827 | 0.280 | 21 | 43058192 | stop gained | G/A | snv | 5 | |||
| rs112735431 | 0.683 | 0.320 | 17 | 80385145 | missense variant | G/A;C | snv | 2.6E-04; 8.0E-06 | 24 | ||
| rs1359880314 | 0.763 | 0.320 | 21 | 45534541 | synonymous variant | C/T | snv | 1.6E-05 | 2.8E-05 | 12 | |
| rs1457092 | 0.790 | 0.320 | 19 | 17193427 | intron variant | C/A | snv | 0.44 | 8 | ||
| rs12325817 | 0.807 | 0.320 | 17 | 17583205 | intron variant | C/A;G;T | snv | 7 | |||
| rs5742905 | 0.701 | 0.360 | 21 | 43063074 | missense variant | A/G | snv | 22 | |||
| rs63750264 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 17 | |||
| rs1237063529 | 0.752 | 0.360 | 21 | 43058894 | missense variant | T/G | snv | 5.6E-06 | 13 | ||
| rs587781858 | 0.742 | 0.360 | 17 | 7669671 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 12 |