| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
| rs734553 | 0.851 | 0.240 | 4 | 9921380 | intron variant | G/A;T | snv | 7 | |||
| rs144246695 | 0.851 | 0.160 | 4 | 83310887 | missense variant | G/A | snv | 8.0E-06 | 4 | ||
| rs766503255 | 0.882 | 0.080 | 17 | 44372408 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
| rs4790694 | 0.882 | 0.160 | 17 | 4723059 | downstream gene variant | A/C | snv | 0.73 | 3 | ||
| rs4522461 | 0.925 | 0.120 | 17 | 4718478 | intron variant | T/G | snv | 0.82 | 2 | ||
| rs879255514 | 0.925 | 0.080 | 17 | 44372407 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs887183646 | 1.000 | 0.080 | 4 | 109976079 | missense variant | C/T | snv | 3.2E-05 | 2.8E-05 | 1 | |
| rs1052533574 | 1.000 | 0.080 | 17 | 44386063 | missense variant | A/G | snv | 1 | |||
| rs1344532070 | 1.000 | 0.080 | 17 | 44375894 | missense variant | A/G | snv | 8.2E-06 | 7.0E-06 | 1 | |
| rs1361881161 | 1.000 | 0.080 | 17 | 44385698 | missense variant | G/A | snv | 1 | |||
| rs137852906 | 1.000 | 0.080 | 17 | 44380004 | stop gained | G/A;T | snv | 1.6E-05; 8.0E-06 | 1 | ||
| rs137852907 | 1.000 | 0.080 | 17 | 44384567 | missense variant | C/T | snv | 1 | |||
| rs137852908 | 1.000 | 0.080 | 17 | 44383630 | missense variant | C/T | snv | 1 | |||
| rs137852910 | 1.000 | 0.080 | 17 | 44383640 | missense variant | C/T | snv | 8.8E-06 | 1 | ||
| rs137852911 | 1.000 | 0.080 | 17 | 44385193 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
| rs1393770089 | 1.000 | 0.080 | 17 | 44375674 | missense variant | G/A | snv | 1 | |||
| rs1555613692 | 1.000 | 0.080 | 17 | 44378360 | splice donor variant | A/G | snv | 1 | |||
| rs74475415 | 1.000 | 0.080 | 17 | 44376323 | missense variant | T/G | snv | 8.0E-06 | 1 | ||
| rs746091910 | 1.000 | 0.080 | 17 | 44378642 | splice donor variant | C/T | snv | 5.7E-06 | 1 | ||
| rs75622274 | 1.000 | 0.080 | 17 | 44381058 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
| rs761174160 | 1.000 | 0.080 | 17 | 44377022 | missense variant | G/C | snv | 4.6E-06 | 1 | ||
| rs763330792 | 1.000 | 0.080 | 17 | 44375719 | splice region variant | G/A;C;T | snv | 5.5E-06; 5.5E-06; 5.5E-06 | 1 | ||
| rs763762304 | 1.000 | 0.080 | 17 | 44377012 | missense variant | C/G;T | snv | 4.7E-06; 5.6E-05 | 1 |