| 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 | ||
| rs80356616 | 0.732 | 0.360 | 11 | 17387917 | missense variant | C/T | snv | 19 | |||
| rs4906902 | 0.724 | 0.200 | 15 | 26774621 | intron variant | A/G | snv | 0.15 | 14 | ||
| rs211037 | 0.742 | 0.240 | 5 | 162101274 | synonymous variant | C/T | snv | 0.28 | 0.31 | 14 | |
| rs121909673 | 0.776 | 0.080 | 5 | 162093965 | missense variant | G/A | snv | 10 | |||
| rs1285524167 | 0.807 | 0.280 | 11 | 17475004 | missense variant | C/T | snv | 8.0E-06 | 8 | ||
| rs200455852 | 0.851 | 0.200 | 8 | 18064458 | missense variant | T/C;G | snv | 5.8E-05 | 6 | ||
| rs1130183 | 0.827 | 0.160 | 1 | 160041722 | missense variant | G/A | snv | 4.6E-02 | 4.7E-02 | 6 | |
| rs199516560 | 0.851 | 0.200 | 7 | 87600772 | 5 prime UTR variant | G/A | snv | 2.1E-05 | 5 | ||
| rs1805031 | 0.851 | 0.080 | 2 | 151880879 | missense variant | C/A | snv | 4.7E-04 | 7.3E-04 | 5 | |
| rs121918628 | 0.851 | 0.080 | 2 | 165998049 | missense variant | G/T | snv | 5 | |||
| rs121917953 | 0.851 | 0.080 | 2 | 166054677 | missense variant | T/A | snv | 4 | |||
| rs375168720 | 0.882 | 0.120 | 8 | 38253642 | missense variant | G/C | snv | 6.0E-05 | 6.3E-05 | 3 | |
| rs121964976 | 0.882 | 0.160 | 9 | 6589230 | missense variant | C/G;T | snv | 8.7E-05; 2.3E-02 | 3 | ||
| rs1883415 | 0.925 | 0.040 | 6 | 24491247 | intron variant | A/C | snv | 0.34 | 3 | ||
| rs4665630 | 0.925 | 0.080 | 2 | 23675447 | intron variant | C/T | snv | 0.78 | 3 | ||
| rs796052908 | 0.882 | 0.160 | 15 | 89327329 | frameshift variant | AG/- | delins | 4.0E-06 | 1.4E-05 | 3 | |
| rs121917986 | 0.882 | 0.040 | 2 | 166002588 | missense variant | C/G;T | snv | 3 | |||
| rs72823592 | 0.925 | 0.040 | 17 | 48045642 | non coding transcript exon variant | G/A;C | snv | 2 | |||
| rs2499697 | 0.925 | 0.040 | 6 | 34077141 | intron variant | A/C;G | snv | 2 | |||
| rs1939012 | 1.000 | 0.040 | 11 | 102724404 | intron variant | T/C | snv | 0.58 | 2 | ||
| rs2304016 | 0.925 | 0.040 | 2 | 165311993 | intron variant | A/G | snv | 1.2E-02 | 4.8E-03 | 2 | |
| rs1402398 | 1.000 | 0.040 | 2 | 57815106 | intergenic variant | G/A | snv | 0.66 | 1 | ||
| rs2833098 | 1.000 | 0.040 | 21 | 30811678 | upstream gene variant | G/A | snv | 0.59 | 1 | ||
| rs2947349 | 1.000 | 0.040 | 2 | 57832668 | intergenic variant | C/A;G | snv | 1 |