| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10172410 | 1.000 | 0.040 | 2 | 181487841 | intron variant | T/C | snv | 0.45 | 1 | ||
| rs10218792 | 1.000 | 0.040 | 1 | 245587630 | intron variant | T/G | snv | 0.26 | 1 | ||
| rs1024611 | 0.568 | 0.800 | 17 | 34252769 | upstream gene variant | A/G | snv | 0.28 | 63 | ||
| rs1032128 | 1.000 | 0.040 | 8 | 118939534 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs1034528 | 0.882 | 0.120 | 1 | 11189075 | intron variant | G/C | snv | 0.30 | 5 | ||
| rs1034762 | 1.000 | 0.040 | 12 | 47995860 | intron variant | A/C | snv | 0.74 | 0.79 | 1 | |
| rs10401670 | 1.000 | 0.040 | 19 | 7677916 | intron variant | T/C;G | snv | 0.49 | 1 | ||
| rs1042667 | 1.000 | 0.040 | 17 | 72124410 | 3 prime UTR variant | A/C | snv | 0.41 | 0.36 | 3 | |
| rs1044122 | 0.925 | 0.040 | 10 | 126036209 | synonymous variant | A/G | snv | 0.27 | 0.26 | 2 | |
| rs10492367 | 0.882 | 0.040 | 12 | 27862037 | regulatory region variant | G/T | snv | 0.12 | 3 | ||
| rs10502437 | 1.000 | 0.040 | 18 | 23390742 | intron variant | G/A | snv | 0.30 | 1 | ||
| rs1052981 | 1.000 | 0.040 | 7 | 37906899 | 3 prime UTR variant | G/A | snv | 0.70 | 1 | ||
| rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
| rs1062033 | 1.000 | 0.040 | 15 | 51255741 | 5 prime UTR variant | C/G | snv | 0.35 | 1 | ||
| rs10654220 | 1.000 | 0.040 | 12 | 123218875 | intron variant | -/TGT;TGTTGT | delins | 2 | |||
| rs10795550 | 1.000 | 0.040 | 10 | 7562392 | 3 prime UTR variant | T/C;G | snv | 0.88 | 1 | ||
| rs10947262 | 0.925 | 0.040 | 6 | 32405535 | non coding transcript exon variant | C/T | snv | 0.12 | 3 | ||
| rs10948155 | 1.000 | 0.040 | 6 | 44720220 | intergenic variant | T/C | snv | 0.30 | 1 | ||
| rs10948172 | 0.882 | 0.040 | 6 | 44809954 | intron variant | A/G | snv | 0.27 | 3 | ||
| rs10974438 | 0.925 | 0.120 | 9 | 4291928 | intron variant | A/C | snv | 0.29 | 3 | ||
| rs10980705 | 1.000 | 0.040 | 9 | 111040905 | upstream gene variant | C/T | snv | 0.18 | 1 | ||
| rs11031191 | 1.000 | 0.040 | 11 | 30752733 | intergenic variant | G/C;T | snv | 0.27 | 1 | ||
| rs11107957 | 1.000 | 0.040 | 12 | 78038275 | intron variant | A/C | snv | 0.20 | 1 | ||
| rs11177 | 0.851 | 0.080 | 3 | 52687289 | missense variant | G/A | snv | 0.38 | 0.33 | 4 | |
| rs1126464 | 1.000 | 0.040 | 16 | 89637957 | missense variant | G/A;C | snv | 1.3E-05; 0.26 | 4 |