| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
| rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
| rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
| rs17758695 | 18 | 63253621 | intron variant | C/T | snv | 2.1E-02 | 10 | ||||
| rs218265 | 4 | 54542832 | intergenic variant | T/C | snv | 0.21 | 10 | ||||
| rs9977672 | 0.827 | 0.120 | 21 | 39091357 | intergenic variant | G/A | snv | 0.22 | 10 | ||
| rs35979828 | 12 | 54292096 | intron variant | C/T | snv | 5.0E-02 | 9 | ||||
| rs2979489 | 8 | 30423317 | intron variant | G/A;C | snv | 6 | |||||
| rs10858740 | 12 | 88451258 | intergenic variant | A/G;T | snv | 0.56 | 5 | ||||
| rs3809627 | 16 | 30091839 | 5 prime UTR variant | C/A | snv | 0.41 | 5 | ||||
| rs78744187 | 19 | 33263642 | intergenic variant | C/T | snv | 6.8E-02 | 5 | ||||
| rs16928078 | 11 | 2298783 | intron variant | C/T | snv | 0.15 | 4 | ||||
| rs1811069 | 1.000 | 0.040 | 22 | 21627765 | upstream gene variant | T/A;G | snv | 4 | |||
| rs762679 | 8 | 47972876 | missense variant | T/A | snv | 0.87 | 0.88 | 4 | |||
| rs35150201 | 7 | 135661514 | upstream gene variant | T/G | snv | 0.42 | 3 | ||||
| rs609018 | 12 | 3962735 | regulatory region variant | T/A;G | snv | 3 | |||||
| rs72755295 | 1.000 | 0.080 | 1 | 241870961 | intron variant | A/G | snv | 2.1E-02 | 3 | ||
| rs72766630 | 9 | 134061669 | intron variant | G/A;T | snv | 3 | |||||
| rs2502994 | 1 | 23872873 | 3 prime UTR variant | T/A;C | snv | 2 | |||||
| rs371638091 | 12 | 120920824 | downstream gene variant | TT/-;T;TTT | delins | 0.33 | 2 | ||||
| rs3824867 | 11 | 47447017 | intron variant | A/G | snv | 0.59 | 2 |