| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1333049 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 60 | ||
| rs4291 | 0.724 | 0.400 | 17 | 63476833 | upstream gene variant | T/A;C | snv | 20 | |||
| rs387906592 | 0.752 | 0.280 | 10 | 88941309 | missense variant | C/T | snv | 14 | |||
| rs9333025 | 0.851 | 0.200 | 1 | 46931231 | intron variant | C/T | snv | 9.4E-02 | 8 | ||
| rs2359612 | 0.851 | 0.120 | 16 | 31092475 | intron variant | A/G | snv | 0.66 | 7 | ||
| rs1558139 | 0.851 | 0.160 | 19 | 15886754 | intron variant | G/A | snv | 0.46 | 6 | ||
| rs28357984 | 0.851 | 0.160 | MT | 5178 | missense variant | C/A | snv | 6 | |||
| rs9923231 | 0.851 | 0.200 | 16 | 31096368 | upstream gene variant | C/A;G;T | snv | 6 | |||
| rs9332978 | 0.882 | 0.040 | 1 | 46942278 | upstream gene variant | T/C | snv | 7.3E-02 | 5 | ||
| rs1411224107 | 0.882 | 0.160 | 7 | 101128439 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
| rs2968915 | 1.000 | 0.040 | X | 40580182 | intron variant | G/A | snv | 3 | |||
| rs5049 | 1.000 | 0.040 | 1 | 230714337 | intron variant | C/T | snv | 0.16 | 3 | ||
| rs516115 | 12 | 91163515 | intron variant | T/C | snv | 0.38 | 1 | ||||
| rs563985037 | 3 | 39107505 | missense variant | C/T | snv | 4.2E-05 | 1 | ||||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397514624 | 0.925 | 13 | 110187254 | missense variant | G/A;C;T | snv | 1.6E-05; 4.0E-06 | 3 | |||
| rs774229224 | 0.882 | 0.160 | 6 | 160706454 | missense variant | C/A;G | snv | 4.0E-06; 4.0E-06 | 6 | ||
| rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
| rs3783613 | 0.851 | 0.200 | 1 | 100731231 | missense variant | G/A;C | snv | 4.0E-06; 9.9E-03 | 6 | ||
| rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
| rs544456198 | 0.790 | 0.120 | 19 | 11116930 | missense variant | G/T | snv | 8.0E-06 | 2.8E-05 | 9 | |
| rs371237692 | 0.925 | 0.120 | 1 | 204159515 | synonymous variant | A/G | snv | 8.0E-06 | 3.5E-05 | 5 | |
| rs112735431 | 0.683 | 0.320 | 17 | 80385145 | missense variant | G/A;C | snv | 2.6E-04; 8.0E-06 | 24 | ||
| rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
| rs4961 | 0.683 | 0.400 | 4 | 2904980 | missense variant | G/A;T | snv | 1.2E-05; 0.20 | 27 |