| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10494251 | 0.851 | 0.040 | 1 | 147552120 | intron variant | C/T | snv | 5.8E-02 | 4 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs1541187 | 0.882 | 0.040 | 1 | 147579693 | intron variant | C/G;T | snv | 3 | |||
| rs1805087 | 0.496 | 0.800 | 1 | 236885200 | missense variant | A/G | snv | 0.20 | 0.21 | 135 | |
| rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs6586354 | 0.851 | 0.040 | 1 | 234897489 | intron variant | G/A | snv | 0.25 | 4 | ||
| rs672607 | 0.851 | 0.040 | 1 | 147581540 | intron variant | G/A | snv | 0.12 | 4 | ||
| rs688325 | 0.851 | 0.040 | 1 | 147605490 | intron variant | G/A | snv | 0.19 | 4 | ||
| rs821616 | 0.752 | 0.200 | 1 | 232008852 | missense variant | A/T | snv | 0.26 | 0.29 | 13 | |
| rs946903 | 0.882 | 0.040 | 1 | 147625465 | 3 prime UTR variant | T/C | snv | 0.25 | 3 | ||
| rs12476147 | 0.851 | 0.040 | 2 | 184936178 | missense variant | A/T | snv | 0.66 | 0.59 | 4 | |
| rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
| rs2302045 | 0.851 | 0.040 | 2 | 241081801 | splice region variant | G/A | snv | 7.6E-02 | 1.0E-01 | 4 | |
| rs231779 | 0.827 | 0.160 | 2 | 203869764 | intron variant | C/T | snv | 0.41 | 5 | ||
| rs139459337 | 0.882 | 0.040 | 3 | 114997018 | intron variant | C/T | snv | 4.7E-02 | 3 | ||
| rs2137947 | 0.882 | 0.040 | 3 | 4989276 | downstream gene variant | C/T | snv | 0.64 | 3 | ||
| rs334558 | 0.701 | 0.320 | 3 | 120094435 | upstream gene variant | A/G | snv | 0.51 | 20 | ||
| rs9862857 | 0.851 | 0.040 | 3 | 30453840 | regulatory region variant | A/G;T | snv | 4 | |||
| rs12649507 | 0.851 | 0.080 | 4 | 55514317 | intron variant | G/A;T | snv | 4 | |||
| rs16875288 | 0.851 | 0.040 | 5 | 5297087 | intron variant | A/T | snv | 0.22 | 4 | ||
| rs17211233 | 0.882 | 0.040 | 5 | 81072944 | intron variant | T/A;C | snv | 4 | |||
| rs17790731 | 0.851 | 0.040 | 5 | 95647825 | 5 prime UTR variant | C/T | snv | 4.9E-02 | 4 | ||
| rs6295 | 0.645 | 0.200 | 5 | 63962738 | intron variant | C/G | snv | 0.49 | 40 | ||
| rs1049353 | 0.630 | 0.600 | 6 | 88143916 | synonymous variant | C/T | snv | 0.21 | 0.20 | 42 |