| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137854498 | 1.000 | 0.120 | 9 | 104798504 | missense variant | G/A;T | snv | 8.0E-06; 8.0E-06 | 3 | ||
| rs9282541 | 0.790 | 0.160 | 9 | 104858554 | missense variant | G/A | snv | 1.3E-02 | 4.4E-03 | 13 | |
| rs2230806 | 0.689 | 0.280 | 9 | 104858586 | missense variant | C/T | snv | 0.32 | 0.39 | 24 | |
| rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 25 | ||
| rs187238 | 0.602 | 0.680 | 11 | 112164265 | intron variant | C/A;G | snv | 48 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs5888 | 0.752 | 0.200 | 12 | 124800202 | synonymous variant | A/G;T | snv | 0.59; 4.0E-06 | 11 | ||
| rs2026458 | 0.882 | 0.080 | 6 | 12825642 | intron variant | C/T | snv | 0.34 | 6 | ||
| rs9349379 | 0.732 | 0.200 | 6 | 12903725 | intron variant | A/G | snv | 0.32 | 19 | ||
| rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
| rs72653706 | 0.695 | 0.480 | 16 | 16163078 | stop gained | G/A | snv | 1.4E-03 | 1.2E-03 | 32 | |
| rs761646500 | 0.925 | 0.080 | 6 | 169237763 | missense variant | C/G | snv | 4.0E-06 | 3 | ||
| rs730880284 | 1 | 169612928 | splice donor variant | C/G;T | snv | 2.8E-05 | 1 | ||||
| rs5361 | 0.623 | 0.720 | 1 | 169731919 | missense variant | T/G | snv | 8.3E-02; 8.0E-06 | 7.8E-02 | 47 | |
| rs1458766475 | 0.637 | 0.680 | 1 | 169732649 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 41 | ||
| rs11573191 | 1.000 | 0.040 | 1 | 20069922 | intron variant | G/A | snv | 0.18 | 2 | ||
| rs1800896 | 0.507 | 0.800 | 1 | 206773552 | intron variant | T/C | snv | 0.41 | 113 | ||
| rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
| rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
| rs1177506410 | 0.776 | 0.240 | 1 | 230706148 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 12 | |
| rs1275805226 | 0.776 | 0.240 | 1 | 230706148 | frameshift variant | G/- | del | 7.0E-06 | 12 | ||
| rs40837 | 0.925 | 0.120 | 16 | 28499524 | 3 prime UTR variant | A/G | snv | 0.43 | 5 | ||
| rs26528 | 0.807 | 0.200 | 16 | 28506388 | intron variant | T/C | snv | 0.43 | 9 | ||
| rs3869109 | 0.851 | 0.160 | 6 | 31216419 | intergenic variant | A/G;T | snv | 5 | |||
| rs2857656 | 0.851 | 0.120 | 17 | 34254988 | upstream gene variant | G/A;C | snv | 5 |