| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs769022609 | 1.000 | 0.080 | 19 | 10092624 | stop gained | T/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs5030809 | 0.776 | 0.320 | 3 | 10142139 | missense variant | T/C | snv | 1.3E-05 | 10 | ||
| rs7964241 | 1.000 | 0.080 | 12 | 101944457 | intron variant | A/G | snv | 0.31 | 1 | ||
| rs12411886 | 0.882 | 0.080 | 10 | 102925542 | intron variant | C/A | snv | 7.8E-02 | 3 | ||
| rs12413409 | 0.790 | 0.200 | 10 | 102959339 | intron variant | G/A | snv | 9.0E-02 | 9 | ||
| rs2230806 | 0.689 | 0.280 | 9 | 104858586 | missense variant | C/T | snv | 0.32 | 0.39 | 24 | |
| rs2374513 | 1.000 | 0.080 | 12 | 105613522 | intergenic variant | C/T | snv | 0.12 | 1 | ||
| rs1930095 | 1.000 | 0.080 | 9 | 108592638 | intergenic variant | T/C | snv | 0.50 | 1 | ||
| rs117537300 | 1.000 | 0.080 | 8 | 10886429 | intergenic variant | G/A | snv | 3.8E-02 | 1 | ||
| rs3783107 | 1.000 | 0.080 | 13 | 110189755 | intron variant | G/A | snv | 0.36 | 2 | ||
| rs201384282 | 1.000 | 0.080 | 19 | 11105562 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 | 1 | |
| rs79461840 | 1.000 | 0.080 | 9 | 112059878 | intron variant | T/C | snv | 7.0E-04 | 1 | ||
| rs78125721 | 1.000 | 0.080 | 3 | 112606830 | intron variant | A/G | snv | 6.6E-03 | 1 | ||
| rs74115822 | 1.000 | 0.080 | 13 | 113277539 | non coding transcript exon variant | G/A | snv | 2.1E-02 | 1 | ||
| rs4979583 | 1.000 | 0.080 | 9 | 115809149 | regulatory region variant | C/A;T | snv | 1 | |||
| rs11536889 | 0.658 | 0.560 | 9 | 117715853 | 3 prime UTR variant | G/C | snv | 0.11 | 27 | ||
| rs3900446 | 1.000 | 0.080 | 5 | 122090980 | intergenic variant | A/G;T | snv | 1 | |||
| rs763497 | 1.000 | 0.080 | 5 | 122091535 | regulatory region variant | A/G | snv | 0.22 | 1 | ||
| rs79134766 | 1.000 | 0.080 | 9 | 124799444 | missense variant | G/A;T | snv | 1.2E-02; 8.5E-06 | 1 | ||
| rs7011138 | 1.000 | 0.080 | 8 | 126909955 | intron variant | A/T | snv | 0.13 | 1 | ||
| rs1380244824 | 1.000 | 0.080 | 9 | 127818812 | synonymous variant | G/A | snv | 4.0E-06 | 1 | ||
| rs1800956 | 1.000 | 0.080 | 9 | 127824342 | missense variant | C/G;T | snv | 9.2E-03; 4.0E-06 | 1 | ||
| rs368800416 | 1.000 | 0.080 | 9 | 127825261 | synonymous variant | G/A | snv | 2.8E-05 | 1.4E-05 | 1 | |
| rs1060504230 | 1.000 | 0.080 | 9 | 127843133 | missense variant | GG/TT | mnv | 1 | |||
| rs371331393 | 1.000 | 0.080 | 11 | 128969377 | stop gained | G/A | snv | 2.8E-05 | 1 |