| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1555457882 | 1.000 | 0.120 | 15 | 74202151 | splice region variant | TT/- | del | 1 | |||
| rs6136 | 0.752 | 0.440 | 1 | 169594713 | missense variant | T/G | snv | 8.2E-02 | 7.5E-02 | 17 | |
| rs118203962 | 1.000 | 0.120 | 15 | 74189244 | missense variant | T/G | snv | 5.4E-04 | 4.1E-04 | 1 | |
| rs2057482 | 0.701 | 0.440 | 14 | 61747130 | 3 prime UTR variant | T/C | snv | 0.84 | 0.80 | 21 | |
| rs372883 | 0.827 | 0.360 | 21 | 29345416 | 3 prime UTR variant | T/C | snv | 0.53 | 5 | ||
| rs1481868107 | 1.000 | 0.120 | 11 | 65654980 | missense variant | T/C | snv | 1 | |||
| rs767494439 | 1.000 | 0.120 | 22 | 17191686 | missense variant | T/C | snv | 2.4E-05 | 1 | ||
| rs770882250 | 1.000 | 0.120 | 11 | 65655757 | missense variant | T/C | snv | 2.4E-05 | 7.0E-06 | 1 | |
| rs869025269 | 1.000 | 0.120 | 15 | 74182448 | missense variant | T/C | snv | 8.3E-06 | 1 | ||
| rs1719217 | 1.000 | 0.120 | 17 | 36080352 | intron variant | T/A;G | snv | 1 | |||
| rs10273639 | 0.776 | 0.280 | 7 | 142749077 | upstream gene variant | T/A;C | snv | 9 | |||
| rs757797666 | 0.925 | 0.240 | 18 | 22171617 | missense variant | G/T | snv | 1.4E-05 | 3 | ||
| rs1800796 | 0.555 | 0.760 | 7 | 22726627 | non coding transcript exon variant | G/C | snv | 9.9E-02 | 74 | ||
| rs121913495 | 0.672 | 0.400 | 20 | 58909366 | missense variant | G/A;T | snv | 28 | |||
| rs772134481 | 1.000 | 0.120 | 15 | 74197360 | missense variant | G/A;T | snv | 3.3E-05; 6.5E-06; 6.5E-06 | 2.8E-05 | 1 | |
| rs774207364 | 1.000 | 0.120 | 12 | 861184 | missense variant | G/A;C | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs121909235 | 0.851 | 0.240 | 10 | 87957919 | missense variant | G/A | snv | 8 | |||
| rs1284110310 | 0.882 | 0.200 | 17 | 39706999 | missense variant | G/A | snv | 7.0E-06 | 5 | ||
| rs1399364791 | 0.882 | 0.240 | 12 | 55967046 | missense variant | G/A | snv | 4.0E-06 | 3 | ||
| rs10919791 | 0.925 | 0.240 | 1 | 199996040 | intergenic variant | G/A | snv | 0.22 | 2 | ||
| rs1569119395 | 0.925 | 0.120 | 22 | 45949926 | stop gained | G/A | snv | 2 | |||
| rs9854771 | 0.925 | 0.240 | 3 | 189790682 | intron variant | G/A | snv | 0.34 | 2 | ||
| rs118203958 | 1.000 | 0.120 | 15 | 74190889 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |
| rs118203959 | 1.000 | 0.120 | 15 | 74180121 | missense variant | G/A | snv | 1.6E-05 | 1 | ||
| rs118203960 | 1.000 | 0.120 | 15 | 74180153 | missense variant | G/A | snv | 1.2E-05 | 3.5E-05 | 1 |