| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
| rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
| rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
| rs5275 | 0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv | 55 | |||
| rs5361 | 0.623 | 0.720 | 1 | 169731919 | missense variant | T/G | snv | 8.3E-02; 8.0E-06 | 7.8E-02 | 47 | |
| rs1458766475 | 0.637 | 0.680 | 1 | 169732649 | missense variant | C/G;T | snv | 4.0E-06; 4.0E-06 | 41 | ||
| rs121434596 | 0.677 | 0.440 | 1 | 114716123 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06 | 26 | ||
| rs768623239 | 0.662 | 0.640 | 1 | 109689278 | missense variant | A/G | snv | 1.5E-05 | 26 | ||
| rs2516839 | 0.732 | 0.320 | 1 | 161043331 | 5 prime UTR variant | C/T | snv | 0.49 | 14 | ||
| rs851797 | 0.752 | 0.240 | 1 | 241889740 | 3 prime UTR variant | A/G | snv | 0.72 | 13 | ||
| rs3737787 | 0.763 | 0.280 | 1 | 161039733 | 3 prime UTR variant | G/A | snv | 0.21 | 11 | ||
| rs1467465 | 0.827 | 0.160 | 1 | 27884892 | non coding transcript exon variant | A/G | snv | 0.61 | 7 | ||
| rs17401966 | 0.790 | 0.280 | 1 | 10325413 | intron variant | A/G | snv | 0.24 | 7 | ||
| rs5013329 | 0.827 | 0.160 | 1 | 46349419 | intron variant | C/T | snv | 0.23 | 6 | ||
| rs638820 | 0.827 | 0.160 | 1 | 109667284 | intron variant | G/A | snv | 0.52 | 5 | ||
| rs186724 | 0.882 | 0.120 | 1 | 110018293 | intron variant | C/G;T | snv | 3 | |||
| rs4648551 | 0.882 | 0.120 | 1 | 3716166 | intron variant | G/A | snv | 0.32 | 3 | ||
| rs56318008 | 0.925 | 0.120 | 1 | 22143914 | 5 prime UTR variant | C/T | snv | 0.13 | 3 | ||
| rs6695978 | 0.882 | 0.120 | 1 | 3731781 | intron variant | G/A | snv | 7.3E-02 | 3 | ||
| rs7365052 | 0.882 | 0.120 | 1 | 236786561 | intergenic variant | T/C | snv | 3 | |||
| rs7526063 | 0.882 | 0.120 | 1 | 236808698 | splice region variant | C/T | snv | 3.8E-02 | 5.6E-02 | 3 | |
| rs1002076 | 0.925 | 0.120 | 1 | 10378834 | 3 prime UTR variant | G/A | snv | 0.33 | 2 | ||
| rs10788679 | 0.925 | 0.120 | 1 | 17590467 | intron variant | A/G | snv | 0.59 | 2 | ||
| rs2256787 | 0.925 | 0.120 | 1 | 17566321 | intron variant | A/C | snv | 0.93 | 2 |