| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10924690 | 1.000 | 0.040 | 1 | 246320481 | intron variant | G/A | snv | 0.20 | 2 | ||
| rs11163687 | 1.000 | 0.040 | 1 | 83199436 | intergenic variant | A/G | snv | 9.6E-02 | 2 | ||
| rs11166389 | 1.000 | 0.040 | 1 | 100000723 | non coding transcript exon variant | G/A | snv | 0.15 | 2 | ||
| rs111696067 | 1.000 | 0.040 | 12 | 132799954 | intron variant | T/C | snv | 5.3E-04 | 2 | ||
| rs11216930 | 1.000 | 0.040 | 11 | 118618067 | intron variant | A/C | snv | 0.22 | 2 | ||
| rs11583706 | 1.000 | 0.040 | 1 | 238358337 | intron variant | G/T | snv | 0.17 | 2 | ||
| rs11598018 | 1.000 | 0.040 | 10 | 103901557 | intron variant | C/A;T | snv | 2 | |||
| rs11599775 | 1.000 | 0.040 | 10 | 112699938 | intron variant | G/A | snv | 0.27 | 2 | ||
| rs11706832 | 1.000 | 0.040 | 3 | 66452557 | intron variant | A/C;G | snv | 2 | |||
| rs12076373 | 1.000 | 0.040 | 1 | 243688645 | intron variant | G/C | snv | 0.20 | 2 | ||
| rs12088062 | 1.000 | 0.040 | 1 | 244811284 | intergenic variant | C/T | snv | 0.20 | 2 | ||
| rs12125049 | 1.000 | 0.040 | 1 | 60202030 | intergenic variant | C/T | snv | 0.12 | 2 | ||
| rs12723208 | 1.000 | 0.040 | 1 | 211337552 | intron variant | A/G | snv | 0.13 | 2 | ||
| rs1275600 | 1.000 | 0.040 | 12 | 75869771 | intron variant | T/A | snv | 0.47 | 2 | ||
| rs12803321 | 1.000 | 0.040 | 11 | 118609400 | intron variant | G/C;T | snv | 2 | |||
| rs1409785 | 1.000 | 0.040 | 1 | 74782438 | intergenic variant | G/A | snv | 0.65 | 2 | ||
| rs1582417 | 0.925 | 0.040 | 5 | 160470494 | intron variant | A/G | snv | 0.80 | 2 | ||
| rs16838813 | 1.000 | 0.040 | 1 | 4364085 | intergenic variant | G/A;T | snv | 0.11 | 2 | ||
| rs17057846 | 0.925 | 0.040 | 5 | 160475306 | intron variant | G/A | snv | 0.13 | 2 | ||
| rs17110757 | 1.000 | 0.040 | 1 | 54584133 | intron variant | G/A | snv | 0.20 | 2 | ||
| rs2236507 | 1.000 | 0.040 | 20 | 63691653 | intron variant | G/C;T | snv | 2 | |||
| rs2278089 | 1.000 | 0.040 | 2 | 151290158 | upstream gene variant | G/T | snv | 0.69 | 2 | ||
| rs2427824 | 1.000 | 0.040 | 1 | 159295272 | intron variant | T/C | snv | 0.79 | 2 | ||
| rs2494262 | 1.000 | 0.040 | 1 | 159283882 | upstream gene variant | C/A;G | snv | 2 | |||
| rs34180180 | 1.000 | 0.040 | 10 | 129466848 | upstream gene variant | G/A | snv | 4.8E-02 | 2 |