| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2808630 | 0.742 | 0.240 | 1 | 159711078 | downstream gene variant | C/T | snv | 0.77 | 13 | ||
| rs2036527 | 0.851 | 0.080 | 15 | 78559273 | regulatory region variant | G/A | snv | 0.29 | 12 | ||
| rs13141641 | 1.000 | 0.040 | 4 | 144585304 | intron variant | T/C | snv | 0.32 | 8 | ||
| rs13118928 | 0.925 | 0.040 | 4 | 144565237 | intron variant | A/G | snv | 0.33 | 7 | ||
| rs1818879 | 0.827 | 0.120 | 7 | 22733108 | downstream gene variant | G/A;C | snv | 7 | |||
| rs7655625 | 1.000 | 0.040 | 4 | 144564763 | intron variant | T/C;G | snv | 7 | |||
| rs2737190 | 0.827 | 0.120 | 9 | 117701903 | upstream gene variant | G/A | snv | 0.52 | 6 | ||
| rs1512288 | 1.000 | 0.040 | 4 | 144570129 | intron variant | G/A | snv | 0.42 | 5 | ||
| rs6817273 | 1.000 | 0.040 | 4 | 144570851 | intron variant | T/A;C | snv | 0.33 | 5 | ||
| rs10429950 | 1.000 | 0.040 | 1 | 218451191 | intergenic variant | T/C | snv | 0.33 | 3 | ||
| rs12459249 | 1.000 | 0.040 | 19 | 40833991 | intron variant | T/C | snv | 0.66 | 3 | ||
| rs12501071 | 1.000 | 0.040 | 4 | 144569207 | intron variant | C/T | snv | 0.42 | 3 | ||
| rs12627514 | 1.000 | 0.040 | 21 | 43339560 | intergenic variant | C/A;G;T | snv | 3 | |||
| rs13140176 | 1.000 | 0.040 | 4 | 144567946 | intron variant | A/G | snv | 0.31 | 3 | ||
| rs1542725 | 1.000 | 0.040 | 4 | 144567182 | intron variant | C/T | snv | 0.31 | 3 | ||
| rs58365910 | 1.000 | 0.040 | 15 | 78556692 | downstream gene variant | T/C | snv | 0.30 | 3 | ||
| rs626750 | 1.000 | 0.040 | 11 | 102850214 | regulatory region variant | G/A | snv | 0.21 | 3 | ||
| rs72736802 | 1.000 | 0.040 | 15 | 78427159 | regulatory region variant | A/T | snv | 0.39 | 3 | ||
| rs72740955 | 1.000 | 0.040 | 15 | 78557437 | intergenic variant | C/T | snv | 0.26 | 3 | ||
| rs10023464 | 1.000 | 0.040 | 4 | 68794020 | intergenic variant | C/T | snv | 0.15 | 2 | ||
| rs11118892 | 1.000 | 0.040 | 1 | 221910253 | intron variant | G/C;T | snv | 2 | |||
| rs114091587 | 1.000 | 0.040 | 5 | 43799826 | intergenic variant | T/C | snv | 9.9E-03 | 2 | ||
| rs114120854 | 1.000 | 0.040 | 4 | 66494949 | intergenic variant | G/A | snv | 2.5E-03 | 2 | ||
| rs114493850 | 1.000 | 0.040 | 5 | 43757677 | intergenic variant | G/T | snv | 9.9E-03 | 2 | ||
| rs114512566 | 1.000 | 0.040 | 5 | 43563335 | intergenic variant | T/C | snv | 1.0E-02 | 2 |