| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6557013 | 1.000 | 0.040 | 5 | 97871838 | intron variant | T/A | snv | 0.97 | 1 | ||
| rs12923310 | 1.000 | 0.040 | 16 | 9694080 | intergenic variant | G/T | snv | 0.32 | 1 | ||
| rs11409738 | 1.000 | 0.040 | 7 | 96090522 | intron variant | A/-;AA;AAA;AAAA | delins | 1 | |||
| rs2626053 | 1.000 | 0.040 | 4 | 95333937 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs2171126 | 1.000 | 0.040 | 12 | 93773444 | intron variant | C/T | snv | 0.49 | 1 | ||
| rs787640 | 1.000 | 0.040 | 10 | 93364916 | intron variant | G/A;C | snv | 1 | |||
| rs614332 | 1.000 | 0.040 | 11 | 93101032 | intergenic variant | C/T | snv | 0.62 | 1 | ||
| rs13301537 | 0.925 | 0.040 | 9 | 92466765 | intron variant | A/G | snv | 0.38 | 2 | ||
| rs330050 | 1.000 | 0.040 | 8 | 9230169 | intron variant | G/C;T | snv | 1 | |||
| rs150365637 | 1.000 | 0.040 | 8 | 9222261 | intron variant | -/T | delins | 0.13 | 1 | ||
| rs12885713 | 0.827 | 0.200 | 14 | 90397013 | intron variant | C/A;G;T | snv | 5 | |||
| rs200818100 | 1.000 | 0.040 | 8 | 89762965 | missense variant | A/C;G | snv | 4.7E-04 | 4.2E-04 | 1 | |
| rs1126464 | 1.000 | 0.040 | 16 | 89637957 | missense variant | G/A;C | snv | 1.3E-05; 0.26 | 4 | ||
| rs1800682 | 0.637 | 0.440 | 10 | 88990206 | non coding transcript exon variant | A/G | snv | 0.54 | 32 | ||
| rs2234767 | 0.649 | 0.280 | 10 | 88989499 | intron variant | G/A;T | snv | 0.15 | 30 | ||
| rs1876836 | 1.000 | 0.040 | 8 | 8824246 | intron variant | T/A;C | snv | 1 | |||
| rs3830675 | 1.000 | 0.040 | 10 | 87931195 | intron variant | -/TCTTA | delins | 3 | |||
| rs1404866 | 1.000 | 0.040 | 12 | 84970700 | intergenic variant | G/A;T | snv | 1 | |||
| rs225014 | 0.695 | 0.400 | 14 | 80203237 | missense variant | T/C | snv | 0.41 | 0.39 | 22 | |
| rs2979715 | 1.000 | 0.040 | 8 | 79650024 | intron variant | C/T | snv | 0.77 | 1 | ||
| rs80057746 | 1.000 | 0.040 | 4 | 78701519 | intergenic variant | C/T | snv | 1.7E-02 | 1 | ||
| rs11107957 | 1.000 | 0.040 | 12 | 78038275 | intron variant | A/C | snv | 0.20 | 1 | ||
| rs1149620 | 1.000 | 0.040 | 11 | 76795528 | intron variant | T/A | snv | 0.50 | 1 | ||
| rs10401670 | 1.000 | 0.040 | 19 | 7677916 | intron variant | T/C;G | snv | 0.49 | 1 | ||
| rs769389061 | 0.925 | 0.120 | 19 | 7670321 | missense variant | G/A;C | snv | 2 |