| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4810485 | 0.732 | 0.480 | 20 | 46119308 | intron variant | T/A;G | snv | 16 | |||
| rs30187 | 0.732 | 0.360 | 5 | 96788627 | missense variant | T/A;C | snv | 0.62 | 14 | ||
| rs28940579 | 0.732 | 0.440 | 16 | 3243310 | missense variant | A/G;T | snv | 2.2E-03; 4.0E-06 | 13 | ||
| rs2227981 | 0.763 | 0.400 | 2 | 241851121 | synonymous variant | A/C;G | snv | 1.6E-04; 0.63 | 12 | ||
| rs2488457 | 0.763 | 0.480 | 1 | 113872746 | intron variant | G/A;C | snv | 11 | |||
| rs3024490 | 0.742 | 0.520 | 1 | 206771966 | intron variant | A/C;G;T | snv | 11 | |||
| rs2293152 | 0.763 | 0.480 | 17 | 42329511 | intron variant | G/A;C;T | snv | 2.8E-05; 0.59; 1.6E-05 | 10 | ||
| rs3853839 | 0.752 | 0.480 | X | 12889539 | 3 prime UTR variant | C/G;T | snv | 10 | |||
| rs1800779 | 0.763 | 0.320 | 7 | 150992855 | intron variant | G/A;C | snv | 9 | |||
| rs3789604 | 0.776 | 0.360 | 1 | 113812320 | synonymous variant | T/A;C;G | snv | 8.5E-06; 1.3E-05; 0.17 | 9 | ||
| rs11230563 | 0.790 | 0.360 | 11 | 61008737 | missense variant | C/G;T | snv | 4.2E-06; 0.31 | 8 | ||
| rs121908147 | 0.807 | 0.280 | 1 | 247424041 | missense variant | G/A;C | snv | 8.3E-03; 4.0E-06 | 7 | ||
| rs1554286 | 0.790 | 0.320 | 1 | 206770888 | 5 prime UTR variant | A/G;T | snv | 0.72 | 7 | ||
| rs104895094 | 0.851 | 0.320 | 16 | 3243403 | missense variant | T/A;C | snv | 8.0E-06; 5.2E-03 | 5 | ||
| rs4947296 | 0.851 | 0.440 | 6 | 31090401 | intergenic variant | T/A;C | snv | 5 | |||
| rs758548184 | 0.851 | 0.240 | 16 | 50699557 | missense variant | G/C | snv | 5 | |||
| rs10863888 | 0.851 | 0.280 | 1 | 211329427 | intron variant | A/C;G;T | snv | 4 | |||
| rs12569232 | 0.882 | 0.280 | 1 | 211379722 | intron variant | G/C;T | snv | 4 | |||
| rs17482078 | 0.882 | 0.240 | 5 | 96783162 | missense variant | C/G;T | snv | 2.8E-05; 0.15 | 4 | ||
| rs2838519 | 0.851 | 0.280 | 21 | 44195140 | intron variant | G/A;C | snv | 4 | |||
| rs762421 | 0.851 | 0.360 | 21 | 44195678 | intron variant | G/A | snv | 4 | |||
| rs76481776 | 0.925 | 0.200 | 7 | 129770387 | non coding transcript exon variant | C/G;T | snv | 5.9E-02 | 4 | ||
| rs104895297 | 0.882 | 0.360 | 12 | 109581427 | missense variant | C/T | snv | 3 | |||
| rs104895083 | 0.925 | 0.200 | 16 | 3247166 | missense variant | G/C;T | snv | 4.0E-05; 1.2E-05 | 2 | ||
| rs10515746 | 0.925 | 0.240 | 5 | 157109557 | intron variant | A/C;T | snv | 2 |