| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1086603 | 0.882 | 0.120 | 1 | 147816164 | intergenic variant | G/A | snv | 3.4E-02 | 3 | ||
| rs12289095 | 0.882 | 0.120 | 11 | 82858764 | 5 prime UTR variant | G/A | snv | 0.13 | 3 | ||
| rs12695894 | 0.882 | 0.120 | 3 | 148724853 | intron variant | A/G | snv | 2.7E-02 | 3 | ||
| rs1461347 | 0.882 | 0.120 | 11 | 37191871 | intergenic variant | T/C | snv | 4.5E-02 | 3 | ||
| rs16849542 | 0.882 | 0.120 | 1 | 161816705 | intron variant | A/G | snv | 2.1E-02 | 3 | ||
| rs17138435 | 0.882 | 0.120 | 11 | 79481943 | TF binding site variant | A/C;G | snv | 1.6E-02 | 3 | ||
| rs17167034 | 0.882 | 0.120 | 7 | 88488811 | intron variant | A/G | snv | 1.4E-02 | 3 | ||
| rs17754109 | 0.882 | 0.120 | 9 | 17130158 | upstream gene variant | C/T | snv | 4.7E-02 | 3 | ||
| rs1880381 | 0.882 | 0.120 | 10 | 85762211 | intron variant | C/T | snv | 4.2E-02 | 3 | ||
| rs3899582 | 0.882 | 0.120 | 13 | 29003859 | intron variant | T/G | snv | 1.9E-02 | 3 | ||
| rs455674 | 0.882 | 0.120 | 6 | 39768626 | regulatory region variant | C/G;T | snv | 3 | |||
| rs4801109 | 0.882 | 0.120 | 18 | 54904203 | 3 prime UTR variant | T/C | snv | 0.76 | 3 | ||
| rs4912575 | 0.882 | 0.120 | 3 | 184506142 | intron variant | G/A | snv | 0.84 | 3 | ||
| rs6023560 | 0.882 | 0.120 | 20 | 54743554 | intergenic variant | A/C;G;T | snv | 0.12 | 3 | ||
| rs6670122 | 0.882 | 0.120 | 1 | 156737983 | intron variant | T/C;G | snv | 0.99 | 3 | ||
| rs6822565 | 0.882 | 0.120 | 4 | 147516360 | intron variant | T/C | snv | 0.42 | 3 | ||
| rs7029953 | 0.882 | 0.120 | 9 | 33406299 | intron variant | G/A | snv | 0.14 | 3 | ||
| rs7175718 | 0.882 | 0.120 | 15 | 83900350 | intron variant | A/C | snv | 1.6E-02 | 3 | ||
| rs7935375 | 0.882 | 0.120 | 11 | 4901952 | intron variant | T/C | snv | 3.5E-02 | 3 | ||
| rs8027881 | 0.882 | 0.120 | 15 | 65231343 | upstream gene variant | C/G | snv | 0.27 | 3 |