| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10892173 | 1.000 | 0.040 | 11 | 117801846 | 3 prime UTR variant | C/T | snv | 0.38 | 1 | ||
| rs10936538 | 1.000 | 0.040 | 3 | 167439281 | downstream gene variant | C/A;T | snv | 1 | |||
| rs11145488 | 1.000 | 0.040 | 9 | 69156023 | intron variant | G/A | snv | 0.19 | 1 | ||
| rs111854391 | 0.716 | 0.280 | 9 | 99138006 | stop gained | C/A;T | snv | 4.0E-06 | 18 | ||
| rs11218544 | 1.000 | 0.040 | 11 | 122168344 | intron variant | T/G | snv | 0.15 | 1 | ||
| rs11225395 | 0.776 | 0.360 | 11 | 102725749 | intron variant | A/C;G | snv | 11 | |||
| rs113422242 | 0.763 | 0.240 | 15 | 48510065 | stop gained | G/A | snv | 7.0E-06 | 14 | ||
| rs11606250 | 1.000 | 0.040 | 11 | 40127750 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs11658305 | 1.000 | 0.040 | 17 | 7526004 | intergenic variant | A/C;T | snv | 1 | |||
| rs11743810 | 1.000 | 0.040 | 5 | 138466715 | intron variant | C/T | snv | 0.50 | 0.48 | 1 | |
| rs11873439 | 1.000 | 0.040 | 18 | 69077051 | intergenic variant | A/C | snv | 0.17 | 2 | ||
| rs121912683 | 0.851 | 0.200 | 4 | 185145020 | missense variant | C/A | snv | 4.0E-06 | 7.0E-06 | 9 | |
| rs121912882 | 0.851 | 0.280 | 12 | 47979534 | missense variant | G/A | snv | 4 | |||
| rs12193446 | 0.925 | 0.040 | 6 | 129498893 | intron variant | A/G | snv | 6.4E-02 | 3 | ||
| rs12423791 | 0.925 | 0.040 | 12 | 102465050 | intron variant | G/C | snv | 2.8E-02 | 5 | ||
| rs12517396 | 1.000 | 0.040 | 5 | 44359424 | intron variant | C/A | snv | 4.1E-02 | 1 | ||
| rs12603825 | 1.000 | 0.040 | 17 | 1770111 | intron variant | G/A;T | snv | 1 | |||
| rs12716080 | 0.882 | 0.040 | 5 | 11166836 | intron variant | G/T | snv | 0.39 | 3 | ||
| rs1294950721 | 0.807 | 0.360 | 20 | 10645355 | splice donor variant | C/A;T | snv | 7.0E-06 | 27 | ||
| rs12965607 | 1.000 | 0.040 | 18 | 49864655 | intron variant | T/G | snv | 1.0E-01 | 1 | ||
| rs13129838 | 1.000 | 0.040 | 4 | 79587634 | non coding transcript exon variant | T/C | snv | 0.66 | 1 | ||
| rs131451 | 0.882 | 0.120 | 22 | 23771357 | intron variant | C/T | snv | 0.82 | 4 | ||
| rs1327062642 | 0.827 | 0.200 | 6 | 35509903 | frameshift variant | -/G | delins | 4.0E-06 | 11 | ||
| rs1331463984 | 0.701 | 0.240 | 16 | 2176350 | missense variant | G/A | snv | 33 | |||
| rs13380104 | 1.000 | 0.040 | 15 | 79086479 | intron variant | C/T | snv | 0.43 | 1 |