| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1185333947 | 1.000 | 0.120 | 13 | 99982171 | missense variant | A/C | snv | 7.0E-06 | 1 | ||
| rs181509591 | 1.000 | 0.160 | 4 | 9996817 | missense variant | G/A;C | snv | 1.4E-04; 2.4E-05 | 1 | ||
| rs118203964 | 0.882 | 0.080 | 1 | 99916492 | missense variant | G/C | snv | 1 | |||
| rs886037936 | 1.000 | 14 | 99897194 | missense variant | A/G | snv | 1 | ||||
| rs886037937 | 1.000 | 14 | 99894754 | missense variant | T/C | snv | 1 | ||||
| rs776127501 | 1.000 | 0.160 | 4 | 9985693 | missense variant | G/A | snv | 3.6E-05 | 2.1E-05 | 1 | |
| rs72558202 | 1.000 | 0.080 | 10 | 99845781 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
| rs72558201 | 1.000 | 0.080 | 10 | 99836193 | missense variant | A/G;T | snv | 4.0E-06; 3.6E-05 | 1 | ||
| rs72558200 | 1.000 | 0.080 | 10 | 99836125 | missense variant | G/A | snv | 9.1E-05 | 8.4E-05 | 1 | |
| rs150726175 | 0.776 | 0.200 | 1 | 9982630 | missense variant | G/A | snv | 7.0E-04 | 8.5E-04 | 1 | |
| rs1208495291 | 1.000 | 0.040 | 1 | 9982613 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
| rs778606847 | 1.000 | 0.040 | 1 | 9982577 | missense variant | T/C | snv | 1.2E-05 | 1.4E-05 | 1 | |
| rs368062092 | 1.000 | 0.040 | 1 | 9982571 | missense variant | G/A;T | snv | 4.4E-05 | 1 | ||
| rs375110174 | 1.000 | 0.040 | 1 | 9982570 | missense variant | C/T | snv | 5.2E-05 | 2.8E-05 | 1 | |
| rs142968179 | 1.000 | 0.040 | 1 | 9982480 | missense variant | C/T | snv | 3.6E-05 | 3.5E-05 | 1 | |
| rs748913297 | 1.000 | 0.040 | 1 | 9982403 | missense variant | A/C;G | snv | 1.2E-05 | 1 | ||
| rs757724544 | 1.000 | 0.040 | 1 | 9982393 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
| rs1244511644 | 1.000 | 0.040 | 1 | 9982327 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs28940272 | 1.000 | 0.320 | 8 | 99820031 | missense variant | A/G | snv | 3.2E-03 | 3.9E-03 | 1 | |
| rs56199535 | 1.000 | 0.080 | 10 | 99818820 | missense variant | C/A;G;T | snv | 8.8E-05 | 1 | ||
| rs120074155 | 1.000 | 0.320 | 8 | 99818473 | missense variant | T/C | snv | 1 | |||
| rs180177370 | 1.000 | 0.320 | 8 | 99817685 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs121908322 | 1.000 | 0.160 | 4 | 9980681 | missense variant | G/A | snv | 3.2E-05 | 2.1E-05 | 1 | |
| rs120074153 | 1.000 | 0.320 | 8 | 99784394 | missense variant | G/A | snv | 1 | |||
| rs771336246 | 1.000 | 0.040 | 1 | 9975769 | missense variant | T/G | snv | 1.2E-05 | 1.1E-04 | 1 |