| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs628604 | 1.000 | 0.040 | 19 | 54028370 | upstream gene variant | C/A;G;T | snv | 1 | |||
| rs8015351 | 1.000 | 0.040 | 14 | 49421667 | intergenic variant | A/G;T | snv | 1 | |||
| rs912765 | 1.000 | 0.040 | 1 | 87178264 | intergenic variant | C/T | snv | 0.45 | 1 | ||
| rs12537271 | 1.000 | 0.040 | 7 | 77671409 | intron variant | C/T | snv | 0.36 | 1 | ||
| rs1055356 | 1.000 | 0.040 | 15 | 34855901 | 3 prime UTR variant | T/C | snv | 0.42 | 1 | ||
| rs857240 | 1.000 | 0.040 | 20 | 3094983 | downstream gene variant | T/A;C | snv | 1 | |||
| rs13104011 | 1.000 | 0.040 | 4 | 15805410 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs3756242 | 1.000 | 0.040 | 4 | 15784379 | intron variant | C/A | snv | 0.15 | 1 | ||
| rs6495307 | 1.000 | 0.040 | 15 | 78597979 | intron variant | C/T | snv | 0.39 | 1 | ||
| rs555018 | 1.000 | 0.040 | 15 | 78586900 | intron variant | G/A | snv | 0.64 | 1 | ||
| rs601079 | 1.000 | 0.040 | 15 | 78577237 | intron variant | T/A;G | snv | 1 | |||
| rs883473 | 1.000 | 0.040 | 15 | 32033473 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs6832769 | 1.000 | 0.040 | 4 | 55432027 | 3 prime UTR variant | G/A | snv | 0.68 | 1 | ||
| rs10251794 | 1.000 | 0.040 | 7 | 146988457 | intron variant | T/A | snv | 0.26 | 1 | ||
| rs2267717 | 1.000 | 0.040 | 7 | 30677427 | intron variant | G/A | snv | 0.17 | 1 | ||
| rs1434789 | 1.000 | 0.040 | 20 | 157259 | upstream gene variant | T/G | snv | 0.29 | 1 | ||
| rs970408 | 1.000 | 0.040 | 15 | 26743838 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs16921695 | 1.000 | 0.040 | 8 | 57145096 | intron variant | T/G | snv | 0.33 | 1 | ||
| rs2770378 | 1.000 | 0.040 | 20 | 3072868 | downstream gene variant | G/A | snv | 0.38 | 1 | ||
| rs111339162 | 1.000 | 0.040 | 6 | 154039596 | missense variant | G/A | snv | 2.0E-05 | 1.4E-04 | 1 | |
| rs362584 | 1.000 | 0.040 | 20 | 10273827 | intron variant | G/A | snv | 0.24 | 1 | ||
| rs2270463 | 1.000 | 0.040 | 3 | 8733391 | intron variant | G/T | snv | 0.23 | 1 | ||
| rs1010657 | 1.000 | 0.040 | 10 | 122238202 | intron variant | A/G | snv | 0.35 | 1 | ||
| rs1317926854 | 1.000 | 0.040 | 12 | 72031625 | missense variant | A/G | snv | 1 | |||
| rs709160 | 1.000 | 0.040 | 3 | 12484903 | intron variant | G/C | snv | 0.56 | 1 |