| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057519775 | 1.000 | 0.080 | 9 | 130873028 | missense variant | T/G | snv | 1 | |||
| rs1064156 | 1.000 | 0.080 | 9 | 130878519 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs121913449 | 1.000 | 0.080 | 9 | 130862977 | missense variant | A/T | snv | 1 | |||
| rs121913450 | 1.000 | 0.080 | 9 | 130873016 | missense variant | A/G | snv | 1 | |||
| rs121913453 | 1.000 | 0.080 | 9 | 130862962 | missense variant | G/A | snv | 1 | |||
| rs121913455 | 1.000 | 0.080 | 9 | 130862955 | missense variant | C/G | snv | 1 | |||
| rs121913456 | 1.000 | 0.080 | 9 | 130862943 | missense variant | A/G | snv | 1 | |||
| rs121913457 | 1.000 | 0.080 | 9 | 130873004 | missense variant | T/C | snv | 1 | |||
| rs121913458 | 1.000 | 0.080 | 9 | 130862969 | missense variant | G/C;T | snv | 1 | |||
| rs34549764 | 1.000 | 0.080 | 9 | 130862953 | missense variant | A/G | snv | 2.6E-03 | 2.5E-03 | 1 | |
| rs636832 | 0.790 | 0.400 | 1 | 35897874 | intron variant | G/A | snv | 0.23 | 8 | ||
| rs886063722 | 1.000 | 0.080 | 9 | 136677118 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
| rs141157255 | 0.882 | 0.120 | 12 | 98659331 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 | 3 | |
| rs6931104 | 1.000 | 0.080 | 6 | 151465042 | intron variant | G/A | snv | 0.54 | 1 | ||
| rs532354124 | 1.000 | 0.080 | 1 | 197103274 | missense variant | T/C;G | snv | 1 | |||
| rs3092856 | 0.882 | 0.120 | 11 | 108289005 | missense variant | C/T | snv | 1.2E-02 | 2.2E-02 | 3 | |
| rs111340708 | 0.925 | 0.080 | 12 | 111447548 | intron variant | TGGGGTGGGGTGGGG/-;TGGGG;TGGGGTGGGG;TGGGGTGGGGTGGGGTGGGG;TGGGGTGGGGTGGGGTGGGGTGGGG | delins | 0.52 | 2 | ||
| rs918140013 | 0.925 | 0.080 | 12 | 111447663 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
| rs755796482 | 1.000 | 0.080 | 12 | 111447512 | missense variant | G/A | snv | 4.1E-06 | 8.1E-06 | 1 | |
| rs1801018 | 0.851 | 0.240 | 18 | 63318646 | synonymous variant | T/C | snv | 0.37 | 0.32 | 6 | |
| rs766124888 | 1.000 | 0.080 | 22 | 23253817 | missense variant | C/A;G | snv | 4.0E-06; 4.0E-06 | 1 | ||
| rs768288452 | 1.000 | 0.080 | 22 | 23181822 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
| rs121913370 | 0.763 | 0.360 | 7 | 140753393 | missense variant | T/C;G | snv | 10 | |||
| rs799917 | 0.708 | 0.320 | 17 | 43092919 | missense variant | G/A;C;T | snv | 0.40; 1.6E-05 | 18 | ||
| rs2043211 | 0.653 | 0.480 | 19 | 48234449 | missense variant | A/T | snv | 0.33 | 0.29 | 29 |