| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10795945 | 1.000 | 0.080 | 10 | 12260608 | intergenic variant | T/A;C | snv | 2 | |||
| rs11257655 | 1.000 | 0.080 | 10 | 12265895 | TF binding site variant | C/T | snv | 0.23 | 4 | ||
| rs11558471 | 1.000 | 0.080 | 8 | 117173494 | 3 prime UTR variant | A/G | snv | 0.25 | 5 | ||
| rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 6 | ||
| rs2191349 | 1.000 | 0.080 | 7 | 15024684 | intergenic variant | G/T | snv | 0.54 | 4 | ||
| rs2246012 | 1.000 | 0.080 | 6 | 131577068 | intron variant | T/A;C | snv | 2 | |||
| rs2296172 | 1.000 | 0.080 | 1 | 39370145 | missense variant | A/G;T | snv | 0.19; 8.0E-06 | 4 | ||
| rs2299383 | 1.000 | 0.080 | 7 | 103778399 | intron variant | C/T | snv | 0.41 | 2 | ||
| rs2304130 | 1.000 | 0.080 | 19 | 19678719 | splice region variant | A/G | snv | 0.10 | 0.12 | 5 | |
| rs329122 | 1.000 | 0.080 | 5 | 134528909 | intron variant | G/A | snv | 0.45 | 2 | ||
| rs340874 | 0.882 | 0.080 | 1 | 213985913 | non coding transcript exon variant | T/C | snv | 0.40 | 4 | ||
| rs35261542 | 1.000 | 0.080 | 6 | 20675561 | intron variant | C/A | snv | 0.26 | 3 | ||
| rs3802177 | 1.000 | 0.080 | 8 | 117172786 | 3 prime UTR variant | G/A | snv | 0.24 | 4 | ||
| rs4865796 | 1.000 | 0.080 | 5 | 53976834 | intron variant | G/A | snv | 0.72 | 3 | ||
| rs6947395 | 1.000 | 0.080 | 7 | 69941675 | intron variant | A/T | snv | 0.20 | 2 | ||
| rs7034200 | 1.000 | 0.080 | 9 | 4289050 | intron variant | C/A;G | snv | 3 | |||
| rs7144011 | 1.000 | 0.080 | 14 | 79474040 | intron variant | G/T | snv | 0.21 | 4 | ||
| rs7173964 | 1.000 | 0.080 | 15 | 62104743 | regulatory region variant | G/A | snv | 0.49 | 3 | ||
| rs72892910 | 1.000 | 0.080 | 6 | 50849174 | downstream gene variant | G/T | snv | 0.17 | 2 | ||
| rs7374732 | 1.000 | 0.080 | 3 | 23161963 | regulatory region variant | C/T | snv | 0.73 | 4 | ||
| rs7570971 | 1.000 | 0.080 | 2 | 135080336 | intron variant | C/A | snv | 0.61 | 5 | ||
| rs7578326 | 0.882 | 0.080 | 2 | 226155937 | TF binding site variant | A/G | snv | 0.36 | 3 | ||
| rs7607980 | 1.000 | 0.080 | 2 | 164694691 | missense variant | T/C | snv | 0.11 | 0.13 | 7 | |
| rs76895963 | 1.000 | 0.080 | 12 | 4275678 | intron variant | T/G | snv | 1.5E-02 | 6 | ||
| rs9368222 | 1.000 | 0.080 | 6 | 20686765 | intron variant | C/A;T | snv | 8 |