| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6020157 | 1.000 | 0.040 | 20 | 49975221 | downstream gene variant | G/A | snv | 0.29 | 1 | ||
| rs6677595 | 1.000 | 0.040 | 1 | 152617711 | downstream gene variant | C/G;T | snv | 1 | |||
| rs68080462 | 1.000 | 0.040 | 3 | 18665014 | intron variant | A/C;T | snv | 1 | |||
| rs681323 | 1.000 | 0.040 | 6 | 137797444 | upstream gene variant | A/C;G | snv | 1 | |||
| rs7237497 | 1.000 | 0.040 | 18 | 12777326 | upstream gene variant | T/A;C | snv | 1 | |||
| rs7352944 | 1.000 | 0.040 | 20 | 50016073 | regulatory region variant | T/C | snv | 0.33 | 1 | ||
| rs73818525 | 1.000 | 0.040 | 5 | 159436379 | intron variant | C/T | snv | 7.4E-02 | 1 | ||
| rs744487 | 1.000 | 0.040 | 1 | 234590266 | upstream gene variant | A/C;T | snv | 1 | |||
| rs7516108 | 1.000 | 0.040 | 1 | 152569753 | upstream gene variant | T/C | snv | 0.65 | 1 | ||
| rs75594032 | 1.000 | 0.040 | 3 | 43744082 | regulatory region variant | G/A | snv | 0.22 | 1 | ||
| rs9264082 | 1.000 | 0.040 | 6 | 31233737 | regulatory region variant | T/C | snv | 0.26 | 1 | ||
| rs9305556 | 1.000 | 0.040 | 21 | 34642609 | regulatory region variant | A/G;T | snv | 1 | |||
| rs9481169 | 1.000 | 0.040 | 6 | 111608659 | upstream gene variant | G/T | snv | 0.17 | 1 | ||
| rs9533962 | 1.000 | 0.040 | 13 | 44760058 | regulatory region variant | C/T | snv | 0.47 | 1 | ||
| rs955155 | 1.000 | 0.040 | 19 | 39238839 | upstream gene variant | G/A | snv | 0.20 | 1 | ||
| rs558671948 | 1.000 | 0.040 | 17 | 81121922 | missense variant | C/T | snv | 1.3E-05 | 5.6E-05 | 1 | |
| rs772818947 | 1.000 | 0.040 | 17 | 81122231 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 | 1 | |
| rs550084704 | 1.000 | 0.040 | 17 | 81126523 | missense variant | G/A | snv | 4.0E-05 | 8.4E-05 | 1 | |
| rs4878497 | 1.000 | 0.040 | 9 | 32432976 | intron variant | G/A | snv | 0.51 | 1 | ||
| rs757286802 | 1.000 | 0.040 | 8 | 26864276 | missense variant | C/A | snv | 8.0E-06 | 1 | ||
| rs2276405 | 1.000 | 0.040 | 1 | 159073406 | stop gained | C/A;T | snv | 8.0E-06; 1.5E-02 | 1 | ||
| rs11568070 | 1.000 | 0.040 | 17 | 4641943 | intron variant | G/A | snv | 2.0E-02 | 1 | ||
| rs610037 | 1.000 | 0.040 | 11 | 65779386 | synonymous variant | A/C | snv | 0.45 | 0.52 | 1 | |
| rs2455826 | 1.000 | 0.040 | 3 | 15621553 | intron variant | G/T | snv | 0.26 | 1 | ||
| rs72933970 | 1.000 | 0.040 | 1 | 67095407 | missense variant | T/C | snv | 7.0E-02 | 0.10 | 1 |