| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6768542 | 1.000 | 0.160 | 3 | 41823982 | intron variant | G/A;C | snv | 2 | |||
| rs1016669 | 1.000 | 0.160 | 3 | 41852948 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs10212536 | 1.000 | 0.160 | 3 | 41785534 | intron variant | A/C;G | snv | 1 | |||
| rs1025646 | 1.000 | 0.160 | 3 | 41712930 | intron variant | A/T | snv | 0.26 | 1 | ||
| rs10452020 | 1.000 | 0.160 | 3 | 41774459 | intron variant | A/C;G | snv | 1 | |||
| rs10452022 | 1.000 | 0.160 | 3 | 41774550 | intron variant | G/A;C | snv | 1 | |||
| rs10510729 | 1.000 | 0.160 | 3 | 41790506 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs10510731 | 1.000 | 0.160 | 3 | 41811818 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs10865914 | 1.000 | 0.160 | 3 | 41878007 | intron variant | C/A;G;T | snv | 1 | |||
| rs11129932 | 1.000 | 0.160 | 3 | 41797275 | intron variant | C/A | snv | 0.12 | 1 | ||
| rs11129935 | 1.000 | 0.160 | 3 | 41943711 | intron variant | A/C | snv | 0.13 | 1 | ||
| rs111304140 | 1.000 | 0.160 | 3 | 41765000 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs111419796 | 1.000 | 0.160 | 3 | 41935476 | intron variant | G/A;C | snv | 1 | |||
| rs111465678 | 1.000 | 0.160 | 3 | 41822913 | intron variant | C/A;T | snv | 1 | |||
| rs111634789 | 1.000 | 0.160 | 3 | 41829864 | intron variant | T/C;G | snv | 1 | |||
| rs111708447 | 1.000 | 0.160 | 3 | 41768091 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs111821658 | 1.000 | 0.160 | 3 | 41828974 | intron variant | C/G | snv | 0.23 | 1 | ||
| rs111877184 | 1.000 | 0.160 | 3 | 41775181 | intron variant | G/A;C | snv | 1 | |||
| rs111967505 | 1.000 | 0.160 | 3 | 41831665 | intron variant | C/T | snv | 0.12 | 1 | ||
| rs112059754 | 1.000 | 0.160 | 3 | 41822633 | intron variant | C/A;G;T | snv | 1 | |||
| rs112071272 | 1.000 | 0.160 | 3 | 41781871 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs112245154 | 1.000 | 0.160 | 3 | 41909028 | intron variant | G/T | snv | 0.13 | 1 | ||
| rs112265441 | 1.000 | 0.160 | 3 | 41794576 | intron variant | G/A | snv | 0.13 | 1 | ||
| rs1125203 | 1.000 | 0.160 | 3 | 41719403 | intron variant | T/C | snv | 0.33 | 1 | ||
| rs112736802 | 1.000 | 0.160 | 3 | 41843375 | intron variant | C/G;T | snv | 1 |