| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267607028 | 0.925 | 0.080 | 19 | 35033827 | stop gained | G/A | snv | 8.0E-06 | 2 | ||
| rs267607029 | 0.925 | 0.080 | 19 | 35033828 | stop gained | G/A | snv | 2 | |||
| rs1064794243 | 0.851 | 0.200 | 17 | 63941169 | missense variant | A/T | snv | 5 | |||
| rs140704891 | 1.000 | 0.080 | 17 | 8289059 | stop gained | G/A;T | snv | 4.0E-06; 4.0E-03 | 1 | ||
| rs370613922 | 1.000 | 0.080 | 17 | 8289425 | missense variant | G/A;C | snv | 1.6E-05 | 1 | ||
| rs751751942 | 1.000 | 0.080 | 17 | 8289312 | missense variant | G/A;C | snv | 4.0E-06; 3.2E-05 | 1 | ||
| rs201375192 | 1.000 | 0.080 | 15 | 73367687 | missense variant | G/A | snv | 3.8E-04 | 1.1E-04 | 1 | |
| rs72554071 | 0.882 | 0.280 | 12 | 21765733 | missense variant | G/A;C | snv | 1.8E-03; 4.0E-06 | 4 | ||
| rs1373685560 | 1.000 | 0.080 | 12 | 2608570 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs140389574 | 1.000 | 0.080 | 12 | 69610633 | missense variant | G/A | snv | 2.5E-03 | 4.4E-04 | 1 | |
| rs377504106 | 1.000 | 0.080 | 12 | 32802533 | synonymous variant | T/A;C | snv | 4.0E-06; 1.3E-04 | 1 | ||
| rs762144273 | 1.000 | 0.080 | 12 | 69610454 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs773116244 | 1.000 | 0.080 | 12 | 111453841 | missense variant | T/A;C | snv | 4.1E-06; 8.1E-06 | 1 | ||
| rs121918282 | 0.882 | 0.080 | 11 | 123653773 | missense variant | A/G | snv | 2.0E-04 | 3.5E-04 | 3 | |
| rs147205617 | 1.000 | 0.080 | 11 | 123642563 | missense variant | C/T | snv | 3.1E-04 | 3.1E-04 | 2 | |
| rs587777023 | 1.000 | 0.080 | 11 | 118166903 | missense variant | T/C | snv | 8.0E-06 | 2.1E-05 | 1 | |
| rs774870551 | 0.925 | 0.160 | 10 | 74070712 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 3 | |
| rs150385900 | 1.000 | 0.080 | 10 | 74107316 | missense variant | G/C | snv | 1.1E-03 | 5.2E-04 | 1 | |
| 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 | ||
| rs9388451 | 0.882 | 0.120 | 6 | 125769231 | regulatory region variant | T/A;C | snv | 3 | |||
| rs1166932620 | 1.000 | 0.080 | 6 | 121447016 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
| rs1268070 | 1.000 | 0.080 | 6 | 125720018 | non coding transcript exon variant | C/T | snv | 0.56 | 1 | ||
| rs530633057 | 1.000 | 0.080 | 6 | 121447471 | synonymous variant | C/T | snv | 4.8E-05 | 2.1E-05 | 1 | |
| rs755660650 | 0.827 | 0.120 | 5 | 102498596 | missense variant | G/C | snv | 4.0E-06 | 5 |