| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs11829119 | 0.851 | 0.040 | 12 | 19040597 | intergenic variant | T/A;C | snv | 4 | |||
| rs12649507 | 0.851 | 0.080 | 4 | 55514317 | intron variant | G/A;T | snv | 4 | |||
| rs1344706 | 0.701 | 0.160 | 2 | 184913701 | intron variant | A/C;T | snv | 21 | |||
| rs1541187 | 0.882 | 0.040 | 1 | 147579693 | intron variant | C/G;T | snv | 3 | |||
| rs17154917 | 0.851 | 0.040 | 7 | 81207393 | intergenic variant | G/A;T | snv | 4 | |||
| rs17211233 | 0.882 | 0.040 | 5 | 81072944 | intron variant | T/A;C | snv | 4 | |||
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs746682028 | 0.645 | 0.480 | 11 | 27658414 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 36 | ||
| rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
| rs9862857 | 0.851 | 0.040 | 3 | 30453840 | regulatory region variant | A/G;T | snv | 4 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs16935279 | 0.851 | 0.040 | 8 | 68961217 | intron variant | T/C | snv | 1.9E-02 | 4 | ||
| rs77826363 | 0.882 | 0.040 | 6 | 1128802 | intergenic variant | G/T | snv | 2.2E-02 | 3 | ||
| rs139459337 | 0.882 | 0.040 | 3 | 114997018 | intron variant | C/T | snv | 4.7E-02 | 3 | ||
| rs17790731 | 0.851 | 0.040 | 5 | 95647825 | 5 prime UTR variant | C/T | snv | 4.9E-02 | 4 | ||
| rs17066873 | 0.851 | 0.040 | 13 | 76889874 | non coding transcript exon variant | T/C | snv | 5.4E-02 | 4 | ||
| rs10968749 | 0.851 | 0.040 | 9 | 28752486 | intergenic variant | A/G | snv | 5.5E-02 | 4 | ||
| rs10494251 | 0.851 | 0.040 | 1 | 147552120 | intron variant | C/T | snv | 5.8E-02 | 4 | ||
| rs9364726 | 0.882 | 0.040 | 6 | 164236705 | intergenic variant | A/G | snv | 6.5E-02 | 3 | ||
| rs10994336 | 0.776 | 0.160 | 10 | 60420054 | intron variant | C/T | snv | 7.5E-02 | 12 | ||
| rs17673138 | 0.851 | 0.040 | 8 | 32840440 | intron variant | A/C | snv | 8.6E-02 | 4 | ||
| rs10405744 | 0.851 | 0.040 | 19 | 19948684 | intron variant | G/A | snv | 9.0E-02 | 4 | ||
| rs2302045 | 0.851 | 0.040 | 2 | 241081801 | splice region variant | G/A | snv | 7.6E-02 | 1.0E-01 | 4 | |
| rs2230912 | 0.752 | 0.280 | 12 | 121184393 | missense variant | A/G | snv | 0.13 | 0.12 | 16 |