| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs74161190 | 1.000 | 0.160 | 10 | 130737530 | intergenic variant | A/G | snv | 1.9E-02 | 1 | ||
| rs75348186 | 1.000 | 0.160 | 10 | 36782685 | intergenic variant | T/C | snv | 1.5E-02 | 1 | ||
| rs78340493 | 1.000 | 0.160 | 4 | 43636179 | intergenic variant | C/A | snv | 5.1E-02 | 1 | ||
| rs1414474 | 1.000 | 0.160 | 1 | 34197810 | missense variant | C/G | snv | 0.20 | 0.20 | 1 | |
| rs73228199 | 1.000 | 0.160 | 3 | 111597517 | intron variant | G/A | snv | 0.11 | 1 | ||
| rs7604016 | 1.000 | 0.160 | 2 | 61965000 | intron variant | T/A;C | snv | 1 | |||
| rs1144964 | 1.000 | 0.160 | 12 | 68944857 | intron variant | G/C;T | snv | 1 | |||
| rs78464534 | 1.000 | 0.160 | 2 | 115234275 | intron variant | C/A;G | snv | 1 | |||
| rs7533141 | 1.000 | 0.160 | 1 | 217543535 | intron variant | T/C | snv | 0.57 | 1 | ||
| rs61811867 | 1.000 | 0.160 | 1 | 154802768 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs11488711 | 1.000 | 0.160 | 1 | 229105486 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs1065386 | 1.000 | 0.160 | 6 | 31356770 | missense variant | G/A;C;T | snv | 0.34; 5.6E-06 | 1 | ||
| rs73050171 | 1.000 | 0.160 | 3 | 174801688 | intron variant | G/A | snv | 0.11 | 1 | ||
| rs74705672 | 1.000 | 0.160 | 8 | 132042380 | intron variant | A/T | snv | 4.9E-02 | 1 | ||
| rs4726066 | 1.000 | 0.160 | 7 | 151625186 | intron variant | G/A;C | snv | 1 | |||
| rs1000708 | 1.000 | 0.160 | 12 | 59689707 | intron variant | C/T | snv | 0.58 | 1 | ||
| rs114921230 | 1.000 | 0.160 | 1 | 226595161 | intron variant | G/A | snv | 3.6E-02 | 1 | ||
| rs3081219 | 1.000 | 0.160 | 15 | 53583969 | intron variant | GAGA/-;GA | delins | 1 | |||
| rs71354195 | 1.000 | 0.160 | 19 | 36385416 | intron variant | G/C | snv | 5.3E-02 | 1 | ||
| rs201584991 | 1.000 | 0.160 | 8 | 124979483 | downstream gene variant | ATT/- | delins | 2.6E-04 | 1 |