| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12456492 | 0.882 | 0.080 | 18 | 43093415 | intron variant | A/G | snv | 0.33 | 1 | ||
| rs12638619 | 1.000 | 0.040 | 3 | 183081454 | intron variant | C/T | snv | 0.17 | 1 | ||
| rs12644119 | 1.000 | 0.040 | 4 | 89682268 | intron variant | C/A | snv | 0.17 | 1 | ||
| rs12645693 | 1.000 | 0.040 | 4 | 15727911 | intron variant | G/A | snv | 8.1E-02 | 1 | ||
| rs12726330 | 1.000 | 0.040 | 1 | 155135691 | splice region variant | G/A;C | snv | 1.1E-02; 3.4E-05 | 1 | ||
| rs12817488 | 1.000 | 0.040 | 12 | 122811747 | intron variant | G/A | snv | 0.39 | 2 | ||
| rs12938476 | 1.000 | 0.040 | 17 | 45735531 | intron variant | T/C | snv | 0.40 | 1 | ||
| rs1296028 | 1.000 | 0.040 | 8 | 11841238 | downstream gene variant | A/G | snv | 0.20 | 1 | ||
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
| rs13227860 | 1.000 | 0.040 | 7 | 22114836 | downstream gene variant | G/A | snv | 0.26 | 1 | ||
| rs132985 | 0.827 | 0.120 | 22 | 38167464 | intron variant | C/T | snv | 0.51 | 1 | ||
| rs1372519 | 1.000 | 0.040 | 4 | 89836158 | 5 prime UTR variant | A/G | snv | 0.77 | 1 | ||
| rs1372520 | 1.000 | 0.040 | 4 | 89836354 | intron variant | T/C | snv | 0.78 | 1 | ||
| rs1396862 | 1.000 | 0.040 | 17 | 45825631 | non coding transcript exon variant | G/A | snv | 0.14 | 2 | ||
| rs1411478 | 0.925 | 0.120 | 1 | 180993146 | intron variant | A/G | snv | 0.56 | 1 | ||
| rs1442190 | 1.000 | 0.040 | 12 | 40971838 | 3 prime UTR variant | G/A | snv | 6.8E-02 | 1 | ||
| rs1468375 | 1.000 | 0.040 | 7 | 145337519 | intergenic variant | C/A;T | snv | 1 | |||
| rs1491942 | 1.000 | 0.040 | 12 | 40227006 | intron variant | C/G | snv | 0.23 | 1 | ||
| rs1504212 | 1.000 | 0.040 | 5 | 53824125 | upstream gene variant | C/A | snv | 0.51 | 1 | ||
| rs1526123 | 1.000 | 0.040 | 17 | 45705974 | intron variant | T/C | snv | 0.55 | 1 | ||
| rs1536076 | 1.000 | 0.040 | 9 | 17731923 | intron variant | T/G | snv | 0.19 | 1 | ||
| rs1545843 | 0.827 | 0.120 | 12 | 84170289 | intron variant | G/A | snv | 0.52 | 1 | ||
| rs1564282 | 1.000 | 0.040 | 4 | 858525 | intron variant | C/T | snv | 8.1E-02 | 1 | ||
| rs1630500 | 1.000 | 0.040 | 1 | 154882579 | intergenic variant | G/A | snv | 5.0E-02 | 1 | ||
| rs1635291 | 1.000 | 0.040 | 17 | 45674547 | intron variant | G/A | snv | 0.69 | 2 |