| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12567209 | 0.807 | 0.080 | 1 | 162066689 | upstream gene variant | G/A | snv | 8.6E-02 | 6 | ||
| rs9388451 | 0.882 | 0.120 | 6 | 125769231 | regulatory region variant | T/A;C | snv | 3 | |||
| rs773116244 | 1.000 | 0.080 | 12 | 111453841 | missense variant | T/A;C | snv | 4.1E-06; 8.1E-06 | 1 | ||
| rs1373685560 | 1.000 | 0.080 | 12 | 2608570 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs1166932620 | 1.000 | 0.080 | 6 | 121447016 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
| rs530633057 | 1.000 | 0.080 | 6 | 121447471 | synonymous variant | C/T | snv | 4.8E-05 | 2.1E-05 | 1 | |
| rs201375192 | 1.000 | 0.080 | 15 | 73367687 | missense variant | G/A | snv | 3.8E-04 | 1.1E-04 | 1 | |
| rs149344567 | 0.925 | 0.120 | 1 | 111776247 | missense variant | C/T | snv | 6.4E-05 | 5.6E-05 | 2 | |
| rs150401343 | 0.925 | 0.080 | 1 | 111780713 | missense variant | G/A | snv | 1.3E-04 | 7.0E-05 | 2 | |
| rs12720441 | 1.000 | 0.080 | 7 | 150950216 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs199473547 | 1.000 | 0.080 | 7 | 150945441 | missense variant | C/T | snv | 1.4E-05 | 1 | ||
| rs1268070 | 1.000 | 0.080 | 6 | 125720018 | non coding transcript exon variant | C/T | snv | 0.56 | 1 | ||
| rs72554071 | 0.882 | 0.280 | 12 | 21765733 | missense variant | G/A;C | snv | 1.8E-03; 4.0E-06 | 4 | ||
| rs10494366 | 0.851 | 0.200 | 1 | 162115895 | intron variant | G/T | snv | 0.54 | 7 | ||
| rs140389574 | 1.000 | 0.080 | 12 | 69610633 | missense variant | G/A | snv | 2.5E-03 | 4.4E-04 | 1 | |
| rs762144273 | 1.000 | 0.080 | 12 | 69610454 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs377504106 | 1.000 | 0.080 | 12 | 32802533 | synonymous variant | T/A;C | snv | 4.0E-06; 1.3E-04 | 1 | ||
| rs3766871 | 0.790 | 0.240 | 1 | 237614784 | missense variant | G/A;T | snv | 4.0E-02 | 9 | ||
| rs6795970 | 0.807 | 0.200 | 3 | 38725184 | missense variant | A/G | snv | 0.65 | 0.70 | 13 | |
| rs10428132 | 0.925 | 0.120 | 3 | 38736063 | intron variant | T/G | snv | 0.67 | 2 | ||
| rs6798015 | 1.000 | 0.080 | 3 | 38757345 | intron variant | C/T | snv | 0.70 | 2 | ||
| rs10428168 | 1.000 | 0.080 | 3 | 38738568 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs11129801 | 1.000 | 0.080 | 3 | 38708884 | intron variant | A/G | snv | 0.71 | 1 | ||
| rs12638572 | 1.000 | 0.080 | 3 | 38746306 | intron variant | A/G;T | snv | 1 | |||
| rs138832868 | 1.000 | 0.080 | 3 | 38713959 | missense variant | C/T | snv | 1.7E-03 | 2.5E-03 | 1 |