| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1564483 | 1.000 | 0.080 | 18 | 63127421 | 3 prime UTR variant | C/T | snv | 0.22 | 4 | ||
| rs2302427 | 1.000 | 0.080 | 7 | 148828812 | missense variant | C/G | snv | 7.8E-02 | 6.0E-02 | 4 | |
| rs1940475 | 1.000 | 0.040 | 11 | 102722517 | missense variant | T/C;G | snv | 0.54 | 4 | ||
| rs3757733 | 1.000 | 0.040 | 7 | 116553675 | intron variant | T/A | snv | 0.26 | 4 | ||
| rs3136558 | 1.000 | 2 | 112833698 | intron variant | A/G | snv | 0.21 | 4 | |||
| rs1044471 | 1.000 | 0.080 | 12 | 1787790 | 3 prime UTR variant | C/T | snv | 0.38 | 4 | ||
| rs7668666 | 1.000 | 4 | 186080138 | intron variant | C/A;T | snv | 4 | ||||
| rs1063538 | 1.000 | 0.080 | 3 | 186856394 | 3 prime UTR variant | T/C | snv | 0.55 | 4 | ||
| rs3735656 | 1.000 | 0.040 | 7 | 1541285 | 3 prime UTR variant | C/G;T | snv | 4 | |||
| rs10226620 | 1.000 | 0.040 | 7 | 1541881 | 3 prime UTR variant | T/C | snv | 0.69 | 4 | ||
| rs2297322 | 1.000 | 0.040 | 13 | 98723927 | missense variant | C/G;T | snv | 0.22 | 4 | ||
| rs121434591 | 1.000 | 5 | 139307669 | missense variant | C/G | snv | 4 | ||||
| rs3789678 | 1.000 | 0.040 | 1 | 230713736 | intron variant | C/T | snv | 0.15 | 4 | ||
| rs36217263 | 1.000 | 0.040 | 13 | 33015697 | upstream gene variant | A/- | del | 0.21 | 4 | ||
| rs211105 | 1.000 | 11 | 18033757 | intron variant | T/G | snv | 0.19 | 4 | |||
| rs760743322 | 1.000 | 0.040 | 21 | 25975997 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
| rs2284411 | 1.000 | 0.040 | 12 | 13713238 | intron variant | C/T | snv | 0.34 | 4 | ||
| rs3917412 | 1.000 | 0.040 | 1 | 169731361 | intron variant | T/A;C;G | snv | 4 | |||
| rs1373863123 | 1.000 | 0.080 | 7 | 5529540 | missense variant | G/A | snv | 4 | |||
| rs2835931 | 1.000 | 0.120 | 21 | 37749345 | intron variant | C/A;T | snv | 4 | |||
| rs477145 | 1.000 | 0.120 | 21 | 31390097 | intron variant | C/A;T | snv | 4 | |||
| rs121908586 | 1.000 | 0.080 | 4 | 54274869 | missense variant | T/A;C | snv | 4 | |||
| rs1452231640 | 1.000 | 0.080 | 8 | 42339015 | missense variant | T/C | snv | 4.0E-06 | 4 | ||
| rs71653619 | 1.000 | 0.040 | 1 | 7970934 | missense variant | G/A | snv | 7.9E-03 | 7.0E-03 | 4 | |
| rs763544450 | 1.000 | 0.080 | 21 | 38445560 | missense variant | T/G | snv | 4.0E-06 | 4 |