| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
| rs2069837 | 0.724 | 0.520 | 7 | 22728408 | intron variant | A/C;G | snv | 18 | |||
| rs3757441 | 0.752 | 0.200 | 7 | 148827660 | intron variant | C/T | snv | 0.80 | 12 | ||
| rs849142 | 0.807 | 0.240 | 7 | 28146272 | intron variant | T/C | snv | 0.39 | 6 | ||
| rs3815652 | 0.925 | 0.160 | 7 | 33873792 | intron variant | C/T | snv | 0.19 | 3 | ||
| rs11918092 | 0.925 | 0.120 | 3 | 134794514 | intron variant | C/A | snv | 0.74 | 2 | ||
| rs1023741 | 1.000 | 0.080 | 10 | 96663139 | intron variant | T/C | snv | 0.14 | 1 | ||
| rs10920654 | 1.000 | 0.080 | 1 | 190162620 | intron variant | C/T | snv | 0.22 | 1 | ||
| rs11574077 | 1.000 | 0.080 | 12 | 47859144 | intron variant | T/C | snv | 3.3E-02 | 1 | ||
| rs12949587 | 1.000 | 0.080 | 17 | 79365094 | intron variant | C/T | snv | 0.13 | 1 | ||
| rs1372330 | 1.000 | 0.080 | 9 | 116757309 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs17053011 | 1.000 | 0.080 | 5 | 155934106 | intron variant | G/T | snv | 0.13 | 1 | ||
| rs17082301 | 1.000 | 0.080 | 4 | 53026989 | intron variant | G/A | snv | 0.16 | 1 | ||
| rs2163746 | 1.000 | 0.080 | 5 | 155918211 | intron variant | A/G | snv | 0.14 | 1 | ||
| rs2327990 | 1.000 | 0.080 | 20 | 16208618 | intron variant | T/C | snv | 0.80 | 1 | ||
| rs2366964 | 1.000 | 0.080 | 3 | 59944946 | intron variant | A/G | snv | 0.16 | 1 | ||
| rs3861289 | 1.000 | 0.080 | 18 | 43111710 | intron variant | C/T | snv | 9.6E-02 | 1 | ||
| rs4239258 | 1.000 | 0.080 | 17 | 7493724 | intron variant | A/G;T | snv | 1 | |||
| rs6110524 | 1.000 | 0.080 | 20 | 15130492 | intron variant | A/G | snv | 0.88 | 1 | ||
| rs7153665 | 1.000 | 0.080 | 14 | 100264583 | intron variant | A/G | snv | 0.63 | 1 | ||
| rs756055 | 1.000 | 0.080 | 14 | 100224841 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs885036 | 1.000 | 0.080 | 2 | 98688331 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs1145724 | 1.000 | 0.080 | 6 | 90477791 | intergenic variant | T/C | snv | 0.27 | 1 | ||
| rs4754687 | 1.000 | 0.080 | 11 | 100559322 | intergenic variant | A/C | snv | 0.75 | 1 | ||
| rs5749032 | 1.000 | 0.080 | 22 | 17313079 | intergenic variant | A/G | snv | 0.37 | 1 |