| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs17879961 | 0.597 | 0.480 | 22 | 28725099 | missense variant | A/C;G | snv | 4.1E-03 | 53 | ||
| rs1057520001 | 0.677 | 0.360 | 17 | 7674886 | missense variant | A/C;G | snv | 23 | |||
| rs213210 | 0.742 | 0.240 | 6 | 33208047 | upstream gene variant | A/C;G | snv | 11 | |||
| rs74790047 | 0.851 | 0.120 | 12 | 6601978 | missense variant | A/C;G | snv | 2.0E-05; 1.2E-04; 5.2E-03 | 1.7E-03 | 7 | |
| rs1800264 | 0.827 | 0.120 | X | 32699141 | missense variant | A/C;G | snv | 5.5E-06; 8.3E-03 | 5 | ||
| rs35755165 | 0.882 | 0.080 | 19 | 40840084 | intron variant | A/C;G | snv | 5 | |||
| rs118137916 | 0.882 | 0.080 | 5 | 35863436 | intron variant | A/C;G | snv | 3 | |||
| rs1410508127 | 0.882 | 0.080 | 10 | 113679831 | missense variant | A/C;G | snv | 3 | |||
| rs6985140 | 0.882 | 0.080 | 8 | 9679917 | non coding transcript exon variant | A/C;G | snv | 8.0E-06; 1.0E-01 | 3 | ||
| rs759156239 | 0.882 | 0.080 | 16 | 2044727 | missense variant | A/C;G | snv | 4.1E-06; 4.1E-06 | 3 | ||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 99 | ||
| rs1057519975 | 0.649 | 0.480 | 17 | 7675209 | missense variant | A/C;G;T | snv | 34 | |||
| rs760043106 | 0.645 | 0.440 | 17 | 7674947 | missense variant | A/C;G;T | snv | 32 | |||
| rs1799977 | 0.662 | 0.440 | 3 | 37012077 | missense variant | A/C;G;T | snv | 0.23 | 28 | ||
| rs1859168 | 0.790 | 0.160 | 7 | 27202740 | non coding transcript exon variant | A/C;G;T | snv | 13 | |||
| rs28399433 | 0.827 | 0.200 | 19 | 40850474 | intron variant | A/C;G;T | snv | 0.10; 4.4E-06 | 7 | ||
| rs3774934 | 0.851 | 0.080 | 4 | 102506319 | intron variant | A/C;G;T | snv | 4 | |||
| rs722864 | 0.882 | 0.080 | 2 | 173118476 | intron variant | A/C;G;T | snv | 3 | |||
| rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
| rs699947 | 0.570 | 0.680 | 6 | 43768652 | upstream gene variant | A/C;T | snv | 67 | |||
| rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 | ||
| rs2273535 | 0.645 | 0.360 | 20 | 56386485 | missense variant | A/C;T | snv | 0.28 | 38 | ||
| rs1447295 | 0.658 | 0.400 | 8 | 127472793 | intron variant | A/C;T | snv | 29 | |||
| rs6505162 | 0.695 | 0.320 | 17 | 30117165 | 5 prime UTR variant | A/C;T | snv | 0.50; 3.1E-05 | 25 |