| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs267606704 | 1.000 | 11 | 119278170 | missense variant | A/C;G | snv | 1 | ||||
| rs121913474 | 0.790 | 0.200 | 10 | 121515260 | missense variant | A/G | snv | 3 | |||
| rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 3 | |||
| rs1219648 | 0.716 | 0.320 | 10 | 121586676 | intron variant | A/G;T | snv | 3 | |||
| rs2981582 | 0.695 | 0.360 | 10 | 121592803 | intron variant | A/G | snv | 0.58 | 3 | ||
| rs1800449 | 0.641 | 0.400 | 5 | 122077513 | missense variant | C/A;T | snv | 4.0E-06; 0.17 | 1 | ||
| rs17251221 | 0.724 | 0.360 | 3 | 122274400 | intron variant | A/G | snv | 0.11 | 2 | ||
| rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 2 | |
| rs7684187 | 4 | 122420004 | intron variant | G/A;C | snv | 1 | |||||
| rs12369179 | 0.851 | 0.120 | 12 | 122479003 | intron variant | C/T | snv | 5.9E-02 | 16 | ||
| rs6844999 | 4 | 122660080 | intron variant | T/G | snv | 0.18 | 1 | ||||
| rs12420422 | 0.851 | 0.120 | 11 | 123009573 | intergenic variant | G/A | snv | 3.4E-02 | 16 | ||
| rs7632505 | 0.827 | 0.120 | 3 | 123019460 | intron variant | A/G | snv | 0.34 | 16 | ||
| rs10865710 | 0.763 | 0.360 | 3 | 12311699 | intron variant | C/G | snv | 0.25 | 1 | ||
| rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 5 | |
| rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 4 | |||
| rs587777472 | 1.000 | 7 | 124863630 | missense variant | T/C | snv | 4.1E-06 | 1 | |||
| rs2980853 | 0.851 | 0.120 | 8 | 125466108 | upstream gene variant | A/C | snv | 0.43 | 16 | ||
| rs1016343 | 0.807 | 0.240 | 8 | 127081052 | non coding transcript exon variant | C/T | snv | 0.20 | 3 | ||
| rs13252298 | 0.827 | 0.160 | 8 | 127082911 | non coding transcript exon variant | A/G | snv | 0.24 | 1 | ||
| rs1456315 | 0.790 | 0.200 | 8 | 127091692 | non coding transcript exon variant | T/A;C | snv | 2 | |||
| rs13254738 | 0.807 | 0.160 | 8 | 127092098 | non coding transcript exon variant | C/A;T | snv | 2 | |||
| rs16901979 | 0.724 | 0.480 | 8 | 127112671 | intron variant | C/A | snv | 0.16 | 3 | ||
| rs34330 | 0.724 | 0.280 | 12 | 12717761 | 5 prime UTR variant | T/C | snv | 0.70 | 1 | ||
| rs188140481 | 0.925 | 0.080 | 8 | 127179427 | non coding transcript exon variant | T/A;C | snv | 1 |