| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11646213 | 0.827 | 0.320 | 16 | 82609046 | intergenic variant | A/T | snv | 0.47 | 6 | ||
| rs1454694 | 0.827 | 0.080 | 4 | 181276794 | intergenic variant | T/C | snv | 0.20 | 4 | ||
| rs9295740 | 0.827 | 0.120 | 6 | 27721723 | intergenic variant | G/A | snv | 0.27 | 4 | ||
| rs10503380 | 1.000 | 0.080 | 8 | 9552985 | upstream gene variant | C/T | snv | 0.25 | 2 | ||
| rs11991621 | 1.000 | 0.080 | 8 | 9549072 | intergenic variant | C/T | snv | 0.18 | 2 | ||
| rs12296850 | 0.925 | 0.080 | 12 | 100426307 | downstream gene variant | A/G | snv | 8.7E-02 | 2 | ||
| rs2270628 | 0.925 | 0.120 | 7 | 45909971 | downstream gene variant | C/T | snv | 0.25 | 2 | ||
| rs6601328 | 1.000 | 0.080 | 8 | 9545693 | regulatory region variant | G/A;C | snv | 2 | |||
| rs7040869 | 1.000 | 0.080 | 9 | 99072866 | downstream gene variant | G/A | snv | 0.11 | 2 | ||
| rs10878232 | 1.000 | 0.080 | 12 | 65128867 | intergenic variant | T/A;C;G | snv | 1 | |||
| rs12000445 | 1.000 | 0.080 | 9 | 23426273 | intron variant | A/G | snv | 0.18 | 1 | ||
| rs12621220 | 1.000 | 0.080 | 2 | 112840678 | non coding transcript exon variant | C/T | snv | 0.24 | 1 | ||
| rs1414493 | 1.000 | 0.080 | 1 | 241523216 | upstream gene variant | A/G | snv | 0.62 | 1 | ||
| rs1957860 | 1.000 | 0.080 | 14 | 53962637 | upstream gene variant | C/T | snv | 0.51 | 1 | ||
| rs4743325 | 1.000 | 0.080 | 9 | 99087445 | intergenic variant | G/T | snv | 0.24 | 1 | ||
| rs6122390 | 1.000 | 0.080 | 20 | 63173912 | intron variant | C/T | snv | 0.27 | 1 | ||
| rs7629386 | 1.000 | 0.080 | 3 | 40925416 | regulatory region variant | C/T | snv | 0.30 | 1 | ||
| rs9660710 | 1.000 | 0.080 | 1 | 1163962 | upstream gene variant | A/C;T | snv | 1 | |||
| rs969088 | 1.000 | 0.080 | 5 | 26389153 | intron variant | G/C | snv | 9.9E-02 | 1 | ||
| rs9909179 | 1.000 | 0.080 | 17 | 13140986 | regulatory region variant | T/C | snv | 0.37 | 1 | ||
| rs750443908 | 1.000 | 0.080 | 10 | 50859904 | missense variant | C/A;T | snv | 6.0E-05; 8.0E-06 | 1 | ||
| rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs979090956 | 0.827 | 0.200 | 7 | 87553822 | missense variant | G/C | snv | 5 | |||
| rs201661522 | 1.000 | 0.080 | 7 | 87539293 | missense variant | A/G | snv | 6.4E-05 | 1.0E-04 | 2 |