| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
| rs1200746244 | 0.807 | 0.080 | 1 | 11801287 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 11 | |
| rs78247304 | 0.925 | 0.040 | 2 | 162446391 | missense variant | C/T | snv | 7.6E-05 | 6.4E-04 | 2 | |
| rs17026688 | 1.000 | 0.040 | 3 | 30845325 | intron variant | C/T | snv | 9.3E-03 | 2 | ||
| rs7619173 | 1.000 | 0.040 | 3 | 181279171 | intron variant | C/T | snv | 0.49 | 1 | ||
| rs6295 | 0.645 | 0.200 | 5 | 63962738 | intron variant | C/G | snv | 0.49 | 40 | ||
| rs5326 | 0.851 | 0.160 | 5 | 175443193 | 5 prime UTR variant | C/T | snv | 0.15 | 6 | ||
| rs11956731 | 1.000 | 0.040 | 5 | 161700816 | intron variant | C/A;T | snv | 1 | |||
| rs13188991 | 1.000 | 0.040 | 5 | 161685998 | synonymous variant | G/A;C | snv | 0.19 | 0.18 | 1 | |
| rs2197414 | 1.000 | 0.040 | 5 | 161681878 | intron variant | G/A;C | snv | 1 | |||
| rs3815762 | 1.000 | 0.040 | 5 | 170788816 | intron variant | T/A | snv | 0.11 | 1 | ||
| rs4868029 | 1.000 | 0.040 | 5 | 170790498 | intron variant | C/T | snv | 0.36 | 1 | ||
| rs4921195 | 1.000 | 0.040 | 5 | 161684582 | intron variant | C/A;T | snv | 1 | |||
| rs953038635 | 0.590 | 0.800 | 6 | 159692720 | missense variant | G/A;T | snv | 8.0E-06 | 51 | ||
| rs2619522 | 0.827 | 0.080 | 6 | 15653418 | intron variant | A/C | snv | 0.26 | 6 | ||
| rs1046943 | 1.000 | 0.040 | 6 | 109462738 | 3 prime UTR variant | A/G | snv | 0.52 | 3 | ||
| rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
| rs854560 | 0.513 | 0.800 | 7 | 95316772 | missense variant | A/C;G;N;T | snv | 0.29 | 113 | ||
| rs781140785 | 0.925 | 0.040 | 7 | 150952801 | missense variant | C/T | snv | 1.2E-05 | 4.2E-05 | 2 | |
| rs12547858 | 1.000 | 0.040 | 8 | 32629535 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs3757933 | 1.000 | 0.040 | 8 | 32747325 | intron variant | G/A | snv | 0.23 | 1 | ||
| rs6468121 | 1.000 | 0.040 | 8 | 32643290 | intron variant | G/T | snv | 0.49 | 1 | ||
| rs722642 | 1.000 | 0.040 | 9 | 78681003 | intergenic variant | T/C | snv | 0.72 | 1 | ||
| rs11001178 | 1.000 | 0.040 | 10 | 74842047 | intron variant | T/C;G | snv | 1 | |||
| rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 |