| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6918631 | 1.000 | 0.040 | 6 | 28344679 | intron variant | C/T | snv | 5.3E-02 | 1 | ||
| rs9295769 | 1.000 | 0.040 | 6 | 28336792 | splice region variant | A/G | snv | 5.2E-02 | 1 | ||
| rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 12 | ||
| rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 7 | |||
| rs3757333 | 1.000 | 0.040 | 6 | 30060829 | non coding transcript exon variant | C/A | snv | 9.8E-02 | 1 | ||
| rs16982520 | 1.000 | 0.040 | 20 | 59183665 | intron variant | A/G | snv | 0.14 | 2 | ||
| rs16948048 | 0.925 | 0.040 | 17 | 49363104 | intron variant | A/G | snv | 0.37 | 3 | ||
| rs9468076 | 1.000 | 0.040 | 6 | 27371111 | upstream gene variant | C/T | snv | 0.16 | 1 | ||
| rs10484404 | 1.000 | 0.040 | 6 | 28087717 | intron variant | C/T | snv | 0.15 | 1 | ||
| rs2106261 | 0.763 | 0.160 | 16 | 73017721 | intron variant | C/G;T | snv | 1 | |||
| rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 3 | ||
| rs411538 | 1.000 | 0.040 | 6 | 28587673 | non coding transcript exon variant | C/T | snv | 3.2E-02 | 1 | ||
| rs911178 | 0.925 | 0.120 | 6 | 28606638 | intron variant | T/C | snv | 0.89 | 1 | ||
| rs7819412 | 0.827 | 0.120 | 8 | 11187652 | intron variant | G/A;T | snv | 1 | |||
| rs4689388 | 0.882 | 0.360 | 4 | 6268329 | upstream gene variant | G/A | snv | 0.64 | 3 | ||
| rs6725887 | 0.851 | 0.080 | 2 | 202881162 | intron variant | T/C | snv | 8.9E-02 | 4 | ||
| rs1063856 | 0.763 | 0.400 | 12 | 6044368 | missense variant | T/C;G | snv | 0.31 | 1 | ||
| rs3818532 | 1.000 | 0.040 | 6 | 33712030 | upstream gene variant | A/G | snv | 0.13 | 1 | ||
| rs9815354 | 0.925 | 0.160 | 3 | 41871159 | intron variant | G/A;T | snv | 3 | |||
| rs46522 | 0.807 | 0.120 | 17 | 48911235 | non coding transcript exon variant | C/T | snv | 0.40 | 1 | ||
| rs3883013 | 1.000 | 0.040 | 15 | 84545426 | intron variant | T/C | snv | 5.6E-05 | 1 | ||
| rs2301241 | 0.827 | 0.160 | 9 | 110257228 | upstream gene variant | G/A;T | snv | 1 | |||
| rs1165668 | 1.000 | 0.040 | 12 | 103924218 | intron variant | G/A | snv | 0.71 | 1 | ||
| rs1165669 | 1.000 | 0.040 | 12 | 103924394 | intron variant | A/G | snv | 0.71 | 1 | ||
| rs471364 | 1.000 | 0.040 | 9 | 15289580 | intron variant | C/T | snv | 0.87 | 3 |