| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11053802 | 1.000 | 0.040 | 12 | 10444608 | intron variant | C/G;T | snv | 1 | |||
| rs11059675 | 1.000 | 0.040 | 12 | 122183779 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs11121129 | 1.000 | 0.040 | 1 | 8208035 | intron variant | G/A | snv | 0.26 | 1 | ||
| rs11135056 | 1.000 | 0.040 | 5 | 159260273 | upstream gene variant | C/T | snv | 0.27 | 1 | ||
| rs114934997 | 1.000 | 0.040 | 5 | 40370622 | intergenic variant | C/A;T | snv | 1 | |||
| rs11568070 | 1.000 | 0.040 | 17 | 4641943 | intron variant | G/A | snv | 2.0E-02 | 1 | ||
| rs11574906 | 1.000 | 0.040 | 9 | 136501661 | intron variant | T/A | snv | 8.5E-02 | 1 | ||
| rs11575234 | 1.000 | 0.040 | 12 | 56350492 | intron variant | C/G;T | snv | 1 | |||
| rs1167846 | 1.000 | 0.040 | 6 | 137022583 | intron variant | T/C | snv | 0.61 | 1 | ||
| rs1167849 | 1.000 | 0.040 | 6 | 137027888 | intron variant | A/G | snv | 0.57 | 1 | ||
| rs11795343 | 1.000 | 0.040 | 9 | 32523739 | intron variant | T/C | snv | 0.41 | 1 | ||
| rs118086960 | 1.000 | 0.040 | 11 | 65825973 | intron variant | A/T | snv | 0.62 | 1 | ||
| rs118179173 | 1.000 | 0.040 | 6 | 31367764 | intron variant | T/A | snv | 3.0E-03 | 1 | ||
| rs11922372 | 1.000 | 0.040 | 3 | 191162345 | intergenic variant | T/C | snv | 0.38 | 1 | ||
| rs12118303 | 1.000 | 0.040 | 1 | 172705957 | intergenic variant | T/C | snv | 0.14 | 1 | ||
| rs12199223 | 1.000 | 0.040 | 6 | 31274954 | intron variant | T/A | snv | 8.6E-02 | 1 | ||
| rs12360861 | 1.000 | 0.040 | 11 | 61009601 | missense variant | G/A | snv | 0.13 | 0.14 | 1 | |
| rs12458130 | 1.000 | 0.040 | 18 | 8667063 | intergenic variant | G/A | snv | 8.9E-02 | 1 | ||
| rs1249564 | 1.000 | 0.040 | 1 | 160466663 | regulatory region variant | A/G;T | snv | 1 | |||
| rs12564022 | 1.000 | 0.040 | 1 | 67205072 | intron variant | C/T | snv | 0.30 | 1 | ||
| rs12580100 | 1.000 | 0.040 | 12 | 56045425 | upstream gene variant | A/G | snv | 0.14 | 1 | ||
| rs12586317 | 1.000 | 0.040 | 14 | 35212966 | intron variant | T/C | snv | 0.19 | 1 | ||
| rs12650590 | 1.000 | 0.040 | 4 | 155618869 | intergenic variant | G/T | snv | 0.14 | 1 | ||
| rs1265112 | 1.000 | 0.040 | 6 | 31150242 | intron variant | T/C | snv | 0.28 | 0.28 | 1 | |
| rs1284037740 | 1.000 | 0.040 | 3 | 122337642 | synonymous variant | C/T | snv | 1 |