| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs886041715 | 0.827 | 0.040 | 16 | 56192353 | missense variant | G/A;C;T | snv | 7 | |||
| rs796052621 | 0.827 | 0.080 | 20 | 63444756 | missense variant | C/T | snv | 6 | |||
| rs3829251 | 0.851 | 0.120 | 11 | 71483513 | intron variant | G/A | snv | 0.21 | 8 | ||
| rs587777606 | 0.851 | 0.160 | 11 | 62691300 | stop gained | G/A | snv | 4.0E-06 | 7.0E-06 | 6 | |
| rs121918807 | 0.851 | 0.080 | 2 | 165994275 | missense variant | G/A | snv | 7.2E-05 | 2.8E-05 | 5 | |
| rs222020 | 0.851 | 0.320 | 4 | 71770555 | intron variant | C/T | snv | 0.72 | 5 | ||
| rs1162306056 | 0.882 | 0.080 | 8 | 132174294 | missense variant | C/T | snv | 5 | |||
| rs2239186 | 0.882 | 0.120 | 12 | 47875627 | intron variant | A/C;G | snv | 0.17 | 5 | ||
| rs483352809 | 0.882 | 0.120 | 19 | 6495754 | missense variant | C/T | snv | 5 | |||
| rs527236031 | 0.882 | 0.080 | 20 | 45424323 | missense variant | C/T | snv | 1.6E-05 | 4.2E-05 | 5 | |
| rs756632799 | 0.882 | 0.080 | 20 | 45416579 | stop gained | G/T | snv | 1.6E-05 | 7.0E-06 | 5 | |
| rs368311455 | 0.882 | 0.200 | 1 | 53211185 | missense variant | C/T | snv | 3.2E-05 | 2.8E-05 | 4 | |
| rs118203933 | 0.925 | 0.360 | 8 | 85473779 | missense variant | C/T | snv | 8.0E-06 | 6 | ||
| rs121918046 | 0.925 | 0.160 | 15 | 89325520 | missense variant | G/A | snv | 1.4E-05 | 4 | ||
| rs281864720 | 0.925 | 0.040 | 2 | 29213994 | missense variant | A/C;G;T | snv | 4 | |||
| rs796052650 | 0.925 | 0.040 | 20 | 63413574 | missense variant | G/A;C | snv | 4 | |||
| rs1562902 | 0.925 | 0.120 | 11 | 14896670 | upstream gene variant | C/T | snv | 0.55 | 3 | ||
| rs767399782 | 0.925 | 0.120 | 19 | 6495736 | missense variant | C/A;T | snv | 4.0E-06 | 3 | ||
| rs12800438 | 1.000 | 0.080 | 11 | 71459957 | non coding transcript exon variant | G/A;T | snv | 5 | |||
| rs1057518443 | 1.000 | 0.040 | X | 120557964 | missense variant | T/C | snv | 3 | |||
| rs1057524792 | 1.000 | 0.040 | 4 | 39467617 | missense variant | T/G | snv | 3 | |||
| rs751866383 | 1.000 | 0.040 | 4 | 39470047 | missense variant | G/T | snv | 4.0E-06 | 3 | ||
| rs771844443 | 1.000 | 0.040 | 2 | 165309194 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
| rs796053150 | 1.000 | 0.040 | 2 | 165386827 | missense variant | A/G | snv | 3 | |||
| rs866291718 | 1.000 | 0.040 | 4 | 39470042 | missense variant | A/G | snv | 3 |