| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11221332 | 0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv | 13 | |||
| rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 5 | |||
| rs13010713 | 0.882 | 0.200 | 2 | 181131318 | intron variant | A/C;G | snv | 5 | |||
| rs13098911 | 0.882 | 0.200 | 3 | 46193709 | intron variant | C/G;T | snv | 5 | |||
| rs13314993 | 0.882 | 0.200 | 3 | 32973977 | regulatory region variant | G/C;T | snv | 5 | |||
| rs1464510 | 0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv | 9 | |||
| rs1544410 | 0.542 | 0.760 | 12 | 47846052 | intron variant | C/A;G;T | snv | 78 | |||
| rs17035378 | 0.882 | 0.200 | 2 | 68371823 | intron variant | T/A;C | snv | 5 | |||
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 46 | ||
| rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
| rs3775291 | 0.602 | 0.640 | 4 | 186082920 | missense variant | C/G;T | snv | 1.2E-04; 0.28 | 51 | ||
| rs396991 | 0.742 | 0.480 | 1 | 161544752 | missense variant | A/C;G;T | snv | 0.33; 4.1E-06 | 14 | ||
| rs4819388 | 0.790 | 0.240 | 21 | 44227538 | 3 prime UTR variant | T/C | snv | 9 | |||
| rs555743307 | 0.695 | 0.440 | 16 | 27342243 | missense variant | G/A;T | snv | 3.6E-05; 2.9E-04 | 20 | ||
| rs6927172 | 0.851 | 0.120 | 6 | 137681038 | intron variant | C/A;G;T | snv | 5 | |||
| rs7523907 | 1.000 | 0.080 | 1 | 167458010 | non coding transcript exon variant | C/A;T | snv | 3 | |||
| rs802734 | 0.827 | 0.280 | 6 | 127957653 | intergenic variant | A/G;T | snv | 7 | |||
| rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 20 | |||
| rs9792269 | 0.882 | 0.200 | 8 | 128252343 | intergenic variant | A/C;G | snv | 5 | |||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs745738344 | 0.653 | 0.600 | 6 | 31576786 | synonymous variant | G/A | snv | 1.6E-05 | 1.4E-05 | 28 | |
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
| rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 46 | |
| rs1799782 | 0.474 | 0.800 | 19 | 43553422 | missense variant | G/A | snv | 9.5E-02 | 7.0E-02 | 151 | |
| rs17810546 | 0.827 | 0.440 | 3 | 159947262 | intron variant | A/G | snv | 8.2E-02 | 7 |