| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs72755233 | 1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 | 5 | ||
| rs4988781 | 15 | 100260635 | intron variant | A/C | snv | 0.68 | 1 | ||||
| rs41310284 | 10 | 100687890 | intergenic variant | C/A;T | snv | 3 | |||||
| rs4846204 | 1 | 10248900 | intron variant | C/T | snv | 9.3E-02 | 2 | ||||
| rs314263 | 6 | 104944870 | intron variant | C/T | snv | 0.69 | 4 | ||||
| rs7523050 | 1.000 | 1 | 108875057 | intron variant | C/A | snv | 0.18 | 5 | |||
| rs12546366 | 8 | 10944636 | intron variant | T/C | snv | 0.56 | 1 | ||||
| rs2273368 | 1 | 112521149 | 3 prime UTR variant | C/G;T | snv | 1 | |||||
| rs6489111 | 12 | 122566471 | intron variant | A/G;T | snv | 1 | |||||
| rs12820906 | 12 | 123008576 | intron variant | A/G | snv | 0.20 | 2 | ||||
| rs13241427 | 1.000 | 7 | 1249003 | regulatory region variant | G/T | snv | 0.72 | 6 | |||
| rs3780327 | 9 | 127183568 | intron variant | A/G;T | snv | 1 | |||||
| rs3812049 | 5 | 128083158 | non coding transcript exon variant | C/A;G;T | snv | 4 | |||||
| rs4733727 | 8 | 129719238 | intron variant | C/T | snv | 0.62 | 1 | ||||
| rs4601795 | 11 | 130859535 | intron variant | T/C | snv | 0.58 | 1 | ||||
| rs543860487 | 7 | 137904839 | intron variant | AAA/-;A;AA;AAAA;AAAAA;AAAAAA | delins | 1 | |||||
| rs356429 | 5 | 139693558 | intron variant | C/T | snv | 0.30 | 1 | ||||
| rs2607733 | 3 | 14103134 | intergenic variant | T/A;C | snv | 1 | |||||
| rs9853018 | 3 | 141383119 | intron variant | C/T | snv | 0.54 | 1 | ||||
| rs6570507 | 0.827 | 0.240 | 6 | 142358435 | intron variant | G/A | snv | 0.47 | 13 | ||
| rs7680661 | 4 | 144643964 | intron variant | G/A | snv | 0.79 | 1 | ||||
| rs112416074 | 7 | 148950668 | intergenic variant | -/G | delins | 0.14 | 1 | ||||
| rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 9 | |
| rs56282717 | 7 | 150960007 | intron variant | G/A | snv | 0.16 | 1 | ||||
| rs2982708 | 6 | 152035085 | intron variant | T/C | snv | 0.40 | 1 |