| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs867120336 | 1.000 | 0.040 | 2 | 10048589 | frameshift variant | -/A | delins | 4.1E-06 | 2 | ||
| rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 213 | |||
| rs36217263 | 1.000 | 0.040 | 13 | 33015697 | upstream gene variant | A/- | del | 0.21 | 4 | ||
| rs10946398 | 0.827 | 0.160 | 6 | 20660803 | intron variant | A/C | snv | 0.40 | 5 | ||
| rs16860234 | 0.925 | 0.080 | 3 | 185793096 | intron variant | A/C | snv | 0.33 | 2 | ||
| rs2275703 | 0.925 | 0.080 | 1 | 160195305 | intron variant | A/C | snv | 0.38 | 3 | ||
| rs3134069 | 0.776 | 0.320 | 8 | 118952749 | upstream gene variant | A/C | snv | 9.6E-02 | 11 | ||
| rs3745297 | 0.790 | 0.120 | 19 | 49154952 | missense variant | A/C | snv | 0.41 | 0.38 | 10 | |
| rs5186 | 0.630 | 0.560 | 3 | 148742201 | 3 prime UTR variant | A/C | snv | 0.23 | 0.21 | 38 | |
| rs1044498 | 0.752 | 0.360 | 6 | 131851228 | missense variant | A/C;G | snv | 0.19 | 15 | ||
| rs2236513 | 1.000 | 0.040 | 17 | 17844052 | 3 prime UTR variant | A/C;G | snv | 0.58 | 2 | ||
| rs779271027 | 1.000 | 0.040 | 20 | 44413723 | missense variant | A/C;G | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 110 | ||
| rs1042615 | 1.000 | 0.040 | 12 | 63150429 | missense variant | A/C;G;T | snv | 0.60; 1.2E-05 | 2 | ||
| rs1800783 | 0.827 | 0.280 | 7 | 150992309 | intron variant | A/C;G;T | snv | 7 | |||
| rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 98 | ||
| rs28936379 | 0.807 | 0.120 | 1 | 226888977 | missense variant | A/C;G;T | snv | 4.0E-06 | 9 | ||
| rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 12 | ||
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 48 | ||
| rs2237895 | 0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv | 10 | |||
| rs6476839 | 0.925 | 0.120 | 9 | 4290823 | intron variant | A/C;T | snv | 2 | |||
| rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
| rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 61 | ||
| rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 17 |