| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs13277254 | 1.000 | 0.080 | 8 | 42694839 | upstream gene variant | G/A | snv | 0.66 | 1 | ||
| rs309850 | 1.000 | 0.080 | 8 | 30015821 | regulatory region variant | T/A | snv | 0.32 | 1 | ||
| rs9298629 | 1.000 | 0.080 | 8 | 42751043 | downstream gene variant | G/A;T | snv | 1 | |||
| rs1465781973 | 1.000 | 0.080 | 11 | 113395026 | missense variant | C/T | snv | 2.0E-05 | 1 | ||
| rs2734849 | 1.000 | 0.080 | 11 | 113399438 | missense variant | A/C;G | snv | 4.5E-06; 0.39 | 1 | ||
| rs777160724 | 1.000 | 0.080 | 11 | 113396169 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
| rs4758416 | 1.000 | 0.080 | 11 | 6412919 | intron variant | C/A;G;T | snv | 1 | |||
| rs958331 | 1.000 | 0.080 | 7 | 2921775 | intron variant | T/C | snv | 0.22 | 1 | ||
| rs10082479 | 1.000 | 0.080 | 10 | 49621173 | intron variant | A/T | snv | 0.23 | 1 | ||
| rs12266458 | 1.000 | 0.080 | 10 | 49639951 | intron variant | C/T | snv | 0.11 | 1 | ||
| rs4838547 | 1.000 | 0.080 | 10 | 49654358 | intron variant | T/C | snv | 0.43 | 1 | ||
| rs2472553 | 1.000 | 0.080 | 8 | 27470994 | missense variant | G/A;T | snv | 0.17 | 1 | ||
| rs3735757 | 1.000 | 0.080 | 8 | 27464080 | intron variant | G/A;C;T | snv | 1 | |||
| rs147586937 | 1.000 | 0.080 | 15 | 78602096 | synonymous variant | G/A | snv | 4.8E-05 | 2.8E-05 | 1 | |
| rs749747912 | 1.000 | 0.080 | 15 | 78618880 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs1044394 | 1.000 | 0.080 | 20 | 63350733 | synonymous variant | A/G | snv | 0.92 | 0.81 | 1 | |
| rs2236196 | 1.000 | 0.080 | 20 | 63346204 | 3 prime UTR variant | G/A;C | snv | 0.71 | 1 | ||
| rs2273504 | 1.000 | 0.080 | 20 | 63356709 | intron variant | G/A;T | snv | 1 | |||
| rs3787137 | 1.000 | 0.080 | 20 | 63347748 | intron variant | G/A | snv | 0.42 | 1 | ||
| rs56175056 | 1.000 | 0.080 | 20 | 63350405 | missense variant | G/A;T | snv | 3.3E-04; 4.0E-06 | 1 | ||
| rs755203 | 1.000 | 0.080 | 20 | 63362912 | intron variant | G/A;C | snv | 0.42 | 1 | ||
| rs4861065 | 1.000 | 0.080 | 4 | 40342378 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs2302762 | 1.000 | 0.080 | 17 | 7455542 | non coding transcript exon variant | T/C | snv | 0.61 | 1 | ||
| rs2302763 | 1.000 | 0.080 | 17 | 7455958 | intron variant | T/C;G | snv | 0.18 | 1 | ||
| rs2302765 | 1.000 | 0.080 | 17 | 7447656 | splice region variant | T/C | snv | 0.18 | 0.17 | 1 |