| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10186133 | 1.000 | 0.040 | 2 | 113079367 | downstream gene variant | G/A;T | snv | 1 | |||
| rs10221742 | 1.000 | 0.040 | 2 | 21196778 | downstream gene variant | G/A | snv | 0.32 | 1 | ||
| rs10495907 | 1.000 | 0.040 | 2 | 43771587 | upstream gene variant | G/A | snv | 0.13 | 1 | ||
| rs10793514 | 1.000 | 0.040 | 10 | 44001523 | intergenic variant | T/C | snv | 0.58 | 1 | ||
| rs10951983 | 1.000 | 0.040 | 7 | 6406396 | downstream gene variant | A/G | snv | 0.15 | 1 | ||
| rs10961206 | 1.000 | 0.040 | 9 | 13724052 | intron variant | A/T | snv | 0.12 | 1 | ||
| rs11022738 | 1.000 | 0.040 | 11 | 13271635 | regulatory region variant | T/C | snv | 0.32 | 1 | ||
| rs11042937 | 1.000 | 0.040 | 11 | 10723847 | upstream gene variant | G/T | snv | 0.59 | 1 | ||
| rs111684993 | 1.000 | 0.040 | 15 | 41144539 | intergenic variant | A/G | snv | 0.32 | 1 | ||
| rs112009435 | 1.000 | 0.040 | 19 | 17736035 | upstream gene variant | G/A;C | snv | 1 | |||
| rs11204892 | 1.000 | 0.040 | 1 | 151795572 | upstream gene variant | A/G;T | snv | 1 | |||
| rs11238907 | 1.000 | 0.040 | 10 | 44192332 | intergenic variant | T/G | snv | 0.25 | 1 | ||
| rs113756303 | 1.000 | 0.040 | 8 | 26245256 | intergenic variant | G/T | snv | 0.16 | 1 | ||
| rs1154556 | 1.000 | 0.040 | Y | 21979249 | intron variant | T/C | snv | 1 | |||
| rs11610422 | 1.000 | 0.040 | 12 | 31259735 | regulatory region variant | A/G | snv | 0.15 | 1 | ||
| rs116161686 | 1.000 | 0.040 | 1 | 210300277 | upstream gene variant | G/A | snv | 9.3E-02 | 1 | ||
| rs11677932 | 1.000 | 0.040 | 2 | 237315312 | TF binding site variant | G/A | snv | 0.28 | 1 | ||
| rs11723436 | 1.000 | 0.040 | 4 | 119980181 | intergenic variant | A/G | snv | 0.25 | 1 | ||
| rs11806316 | 1.000 | 0.040 | 1 | 115210861 | regulatory region variant | G/A | snv | 0.26 | 1 | ||
| rs12441817 | 1.000 | 0.040 | 15 | 74733473 | intergenic variant | T/C | snv | 0.16 | 1 | ||
| rs12495221 | 1.000 | 0.040 | 3 | 48137688 | regulatory region variant | C/G;T | snv | 1 | |||
| rs1254531 | 1.000 | 0.040 | 10 | 44083614 | intergenic variant | C/A;T | snv | 1 | |||
| rs12619842 | 1.000 | 0.040 | 2 | 164088534 | intron variant | G/A;C | snv | 1 | |||
| rs12675257 | 1.000 | 0.040 | 8 | 94267412 | intergenic variant | C/T | snv | 0.11 | 1 | ||
| rs12788925 | 1.000 | 0.040 | 11 | 102931118 | intergenic variant | A/G | snv | 0.32 | 1 |