| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2866611 | 0.851 | 0.120 | 20 | 41322165 | upstream gene variant | A/T | snv | 0.58 | 16 | ||
| rs760762 | 0.851 | 0.120 | 20 | 41147406 | intron variant | C/A;T | snv | 0.59 | 16 | ||
| rs1884613 | 0.807 | 0.200 | 20 | 44351775 | intron variant | C/A;G;T | snv | 7 | |||
| rs4810479 | 1.000 | 0.040 | 20 | 45916409 | upstream gene variant | C/T | snv | 0.68 | 7 | ||
| rs13038305 | 0.925 | 0.080 | 20 | 23629625 | intron variant | C/T | snv | 0.21 | 5 | ||
| rs137853336 | 0.851 | 0.080 | 20 | 44413714 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-05 | 5 | ||
| rs1884614 | 0.882 | 0.080 | 20 | 44351879 | non coding transcript exon variant | C/T | snv | 0.18 | 5 | ||
| rs753285226 | 0.882 | 0.080 | 20 | 44406084 | missense variant | C/A;T | snv | 4.0E-06 | 5 | ||
| rs952497863 | 0.925 | 0.080 | 20 | 44414511 | missense variant | C/T | snv | 4 | |||
| rs200711626 | 0.925 | 0.080 | 20 | 17465411 | missense variant | C/T | snv | 8.8E-05 | 3.6E-04 | 3 | |
| rs200998587 | 0.925 | 0.080 | 20 | 45314116 | missense variant | C/T | snv | 1.7E-03 | 4.0E-04 | 3 | |
| rs3818247 | 0.925 | 0.080 | 20 | 44428840 | intron variant | G/C;T | snv | 3 | |||
| rs4810424 | 0.925 | 0.080 | 20 | 44346383 | intron variant | G/C;T | snv | 3 | |||
| rs763010207 | 0.925 | 0.080 | 20 | 44414531 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 3 | |
| rs773661614 | 0.925 | 0.080 | 20 | 44406076 | missense variant | G/A | snv | 8.0E-06 | 4.2E-05 | 3 | |
| rs1240512008 | 1.000 | 0.040 | 20 | 44413780 | missense variant | G/A | snv | 2 | |||
| rs1309065326 | 1.000 | 0.040 | 20 | 38141383 | missense variant | T/C | snv | 5.4E-06 | 7.0E-06 | 2 | |
| rs181914932 | 1.000 | 0.040 | 20 | 45932640 | non coding transcript exon variant | T/C | snv | 1.6E-02 | 2 | ||
| rs2284912 | 1.000 | 0.040 | 20 | 17457568 | intron variant | T/C | snv | 1.7E-02 | 2 | ||
| rs6044695 | 1.000 | 0.040 | 20 | 17244293 | intron variant | A/T | snv | 0.41 | 2 | ||
| rs753476712 | 1.000 | 0.040 | 20 | 44418452 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs754907741 | 1.000 | 0.040 | 20 | 44414567 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 2 | |
| rs779271027 | 1.000 | 0.040 | 20 | 44413723 | missense variant | A/C;G | snv | 4.0E-06; 8.0E-06 | 2 | ||
| rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
| rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 |