| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2295359 | 1.000 | 0.040 | 1 | 67170267 | intron variant | G/A | snv | 0.32 | 1 | ||
| rs41268474 | 1.000 | 0.040 | 1 | 152720036 | missense variant | G/A;C | snv | 9.5E-02; 2.6E-05 | 1 | ||
| rs56364076 | 1.000 | 0.040 | 17 | 42413017 | intron variant | C/T | snv | 0.58 | 1 | ||
| rs963986 | 1.000 | 0.040 | 17 | 42409561 | intron variant | G/C | snv | 0.15 | 1 | ||
| rs1265112 | 1.000 | 0.040 | 6 | 31150242 | intron variant | T/C | snv | 0.28 | 0.28 | 1 | |
| rs130071 | 1.000 | 0.040 | 6 | 31148433 | synonymous variant | G/A | snv | 0.25 | 0.25 | 1 | |
| rs1576 | 1.000 | 0.040 | 6 | 31142614 | missense variant | G/A;C | snv | 4.0E-06; 0.28 | 1 | ||
| rs746647 | 1.000 | 0.040 | 6 | 31146405 | intron variant | A/G | snv | 0.28 | 1 | ||
| rs1406703700 | 1.000 | 0.040 | 20 | 46122352 | missense variant | G/A | snv | 1 | |||
| rs12360861 | 1.000 | 0.040 | 11 | 61009601 | missense variant | G/A | snv | 0.13 | 0.14 | 1 | |
| rs118086960 | 1.000 | 0.040 | 11 | 65825973 | intron variant | A/T | snv | 0.62 | 1 | ||
| rs34394770 | 1.000 | 0.040 | 13 | 39759232 | intron variant | T/C | snv | 0.29 | 1 | ||
| rs36207871 | 1.000 | 0.040 | 12 | 56290713 | intron variant | AGGAA/- | delins | 0.79 | 1 | ||
| rs10088247 | 1.000 | 0.040 | 8 | 3826677 | intron variant | C/T | snv | 0.76 | 1 | ||
| rs7007032 | 1.000 | 0.040 | 8 | 3821924 | intron variant | C/T | snv | 0.75 | 1 | ||
| rs9987128 | 1.000 | 0.040 | 8 | 3122601 | intron variant | A/G | snv | 0.17 | 1 | ||
| rs1284037740 | 1.000 | 0.040 | 3 | 122337642 | synonymous variant | C/T | snv | 1 | |||
| rs771797724 | 1.000 | 0.040 | 10 | 14908688 | missense variant | T/G | snv | 1.6E-05 | 7.0E-06 | 1 | |
| rs11795343 | 1.000 | 0.040 | 9 | 32523739 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs772341797 | 1.000 | 0.040 | 15 | 48342071 | missense variant | A/G | snv | 4.6E-06 | 1 | ||
| rs2700987 | 1.000 | 0.040 | 7 | 37346633 | intron variant | C/A | snv | 0.60 | 1 | ||
| rs2724013 | 1.000 | 0.040 | 7 | 37349706 | intron variant | G/A;T | snv | 1 | |||
| rs2076346 | 1.000 | 0.040 | 1 | 23757159 | intron variant | T/C | snv | 0.27 | 0.21 | 1 | |
| rs151823 | 1.000 | 0.040 | 5 | 96824289 | intron variant | A/C | snv | 0.90 | 1 | ||
| rs6590334 | 1.000 | 0.040 | 11 | 128533313 | intron variant | T/C | snv | 0.60 | 1 |