| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 39 | |
| rs6679677 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 26 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 12 | ||
| rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 11 | |||
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 8 | ||
| rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 7 | |
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 6 | |
| rs7517847 | 0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 | 6 | ||
| rs800292 | 0.645 | 0.560 | 1 | 196673103 | missense variant | G/A | snv | 0.32 | 0.40 | 6 | |
| rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
| rs17849502 | 0.827 | 0.240 | 1 | 183563445 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 3.4E-02 | 5 | ||
| rs6659932 | 0.827 | 0.240 | 1 | 67336688 | intron variant | A/C | snv | 0.81 | 5 | ||
| rs11586238 | 0.925 | 0.160 | 1 | 116720516 | regulatory region variant | C/G | snv | 0.19 | 4 | ||
| rs1217393 | 0.851 | 0.160 | 1 | 113891324 | intron variant | G/A | snv | 0.42 | 4 | ||
| rs2201841 | 0.716 | 0.440 | 1 | 67228519 | intron variant | A/G;T | snv | 4 | |||
| rs2422345 | 0.851 | 0.160 | 1 | 173368608 | upstream gene variant | G/A | snv | 0.63 | 4 | ||
| rs3761959 | 0.827 | 0.320 | 1 | 157699488 | intron variant | C/A;G;T | snv | 4 | |||
| rs3890745 | 0.925 | 0.200 | 1 | 2622185 | intron variant | T/C | snv | 0.40 | 4 | ||
| rs864537 | 0.925 | 0.200 | 1 | 167442147 | intron variant | A/G | snv | 0.29 | 4 | ||
| rs10489629 | 0.827 | 0.240 | 1 | 67222666 | intron variant | T/C | snv | 0.48 | 3 | ||
| rs17465637 | 0.790 | 0.200 | 1 | 222650187 | intron variant | A/C;G;T | snv | 0.64; 6.4E-06 | 3 | ||
| rs6136 | 0.752 | 0.440 | 1 | 169594713 | missense variant | T/G | snv | 8.2E-02 | 7.5E-02 | 3 | |
| rs7528684 | 0.752 | 0.560 | 1 | 157701026 | upstream gene variant | A/G | snv | 0.57 | 3 | ||
| rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 3 | |||
| rs10889677 | 0.627 | 0.720 | 1 | 67259437 | 3 prime UTR variant | C/A | snv | 0.27 | 2 |