| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs397514638 | 1.000 | 0.120 | 15 | 74181301 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
| rs397514639 | 1.000 | 0.120 | 15 | 74180120 | missense variant | C/A;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
| rs397518484 | 1.000 | 0.120 | 15 | 74181459 | splice acceptor variant | C/T | snv | 7.0E-06 | 1 | ||
| rs606231125 | 1.000 | 0.120 | 15 | 74197785 | frameshift variant | G/- | delins | 1 | |||
| rs606231126 | 1.000 | 0.120 | 15 | 74202216 | frameshift variant | AGT/GG | delins | 1.6E-05 | 1 | ||
| rs606231127 | 1.000 | 0.120 | 15 | 74195371 | frameshift variant | -/C | delins | 4.0E-06; 8.0E-06; 4.0E-06 | 1 | ||
| rs772134481 | 1.000 | 0.120 | 15 | 74197360 | missense variant | G/A;T | snv | 3.3E-05; 6.5E-06; 6.5E-06 | 2.8E-05 | 1 | |
| rs869025269 | 1.000 | 0.120 | 15 | 74182448 | missense variant | T/C | snv | 8.3E-06 | 1 | ||
| rs1430937516 | 1.000 | 0.120 | 7 | 76510939 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs774207364 | 1.000 | 0.120 | 12 | 861184 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs10919791 | 0.925 | 0.240 | 1 | 199996040 | intergenic variant | G/A | snv | 0.22 | 2 | ||
| rs67437265 | 0.925 | 0.160 | 4 | 71022523 | missense variant | C/T | snv | 1.8E-02 | 2.3E-02 | 2 | |
| rs2242241 | 0.925 | 0.200 | 8 | 21909370 | missense variant | A/C | snv | 1.0E-02 | 7.9E-03 | 2 | |
| rs11845046 | 1.000 | 0.120 | 14 | 39246997 | missense variant | A/G | snv | 0.22 | 0.20 | 2 | |
| rs191544901 | 0.925 | 0.240 | 1 | 155187241 | missense variant | C/A;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs763861742 | 0.925 | 0.240 | 1 | 155187268 | missense variant | C/G;T | snv | 1.2E-05 | 2 | ||
| rs1374154597 | 1.000 | 0.120 | 3 | 136023097 | frameshift variant | -/G | delins | 2 | |||
| rs397518481 | 0.925 | 0.120 | 3 | 25501230 | stop gained | C/G;T | snv | 2 | |||
| rs9854771 | 0.925 | 0.240 | 3 | 189790682 | intron variant | G/A | snv | 0.34 | 2 | ||
| rs1569119395 | 0.925 | 0.120 | 22 | 45949926 | stop gained | G/A | snv | 2 | |||
| rs11125529 | 0.882 | 0.280 | 2 | 54248729 | intron variant | C/A;T | snv | 3 | |||
| rs757797666 | 0.925 | 0.240 | 18 | 22171617 | missense variant | G/T | snv | 1.4E-05 | 3 | ||
| rs1399364791 | 0.882 | 0.240 | 12 | 55967046 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
| rs151341424 | 0.925 | 0.120 | 15 | 74190856 | missense variant | CC/TT | mnv | 3 | |||
| rs7675998 | 0.827 | 0.360 | 4 | 163086668 | intergenic variant | A/G;T | snv | 5 |