| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs104893755 | 0.851 | 0.200 | 3 | 87259959 | missense variant | G/A | snv | 5 | |||
| rs121918117 | 0.851 | 0.160 | 7 | 30969116 | stop gained | G/A;T | snv | 1.8E-04 | 4 | ||
| rs121917883 | 0.851 | 0.160 | 3 | 172447803 | missense variant | G/A;T | snv | 2.8E-05 | 4 | ||
| rs137853223 | 0.851 | 0.160 | 17 | 63917337 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
| rs121918118 | 0.882 | 0.120 | 7 | 30971183 | missense variant | T/A | snv | 2.4E-05 | 2.8E-05 | 3 | |
| rs104893742 | 0.882 | 0.160 | 3 | 57198405 | missense variant | C/T | snv | 8.0E-06 | 2.8E-05 | 3 | |
| rs763850922 | 0.925 | 0.120 | 17 | 63917760 | splice region variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
| rs137904970 | 0.925 | 0.120 | 9 | 136200607 | missense variant | C/T | snv | 3.2E-05 | 1.4E-05 | 2 | |
| rs749318884 | 0.925 | 0.120 | 1 | 180248431 | missense variant | G/A | snv | 8.4E-05 | 3.5E-05 | 2 | |
| rs6181 | 1.000 | 0.120 | 5 | 42699920 | missense variant | G/A | snv | 2.4E-04 | 9.8E-04 | 1 | |
| rs200743419 | 1.000 | 0.120 | 7 | 30977322 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs112180170 | 1.000 | 0.120 | X | 140505047 | missense variant | C/G;T | snv | 3.1E-05; 2.9E-03 | 1 |