| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
| rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
| rs1205 | 0.602 | 0.680 | 1 | 159712443 | 3 prime UTR variant | C/T | snv | 0.30 | 46 | ||
| rs2234922 | 0.630 | 0.440 | 1 | 225838705 | missense variant | A/G;T | snv | 0.19; 2.8E-05 | 42 | ||
| rs4950928 | 0.653 | 0.560 | 1 | 203186754 | upstream gene variant | G/A;C;T | snv | 33 | |||
| rs2808630 | 0.742 | 0.240 | 1 | 159711078 | downstream gene variant | C/T | snv | 0.77 | 13 | ||
| rs1410996 | 0.807 | 0.240 | 1 | 196727803 | intron variant | G/A | snv | 0.46 | 11 | ||
| rs2274700 | 0.776 | 0.240 | 1 | 196713817 | synonymous variant | G/A;C;T | snv | 0.44 | 11 | ||
| rs3811381 | 0.763 | 0.240 | 1 | 207616743 | missense variant | C/A;G | snv | 8.0E-06; 0.24 | 11 | ||
| rs10737680 | 0.827 | 0.080 | 1 | 196710325 | intron variant | A/C | snv | 0.44 | 9 | ||
| rs1329428 | 0.807 | 0.160 | 1 | 196733680 | intron variant | C/T | snv | 0.44 | 9 | ||
| rs748500299 | 0.790 | 0.200 | 1 | 186675960 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 8 | ||
| rs10922109 | 0.827 | 0.080 | 1 | 196735502 | intron variant | C/A | snv | 0.46 | 6 | ||
| rs3753395 | 0.882 | 0.120 | 1 | 196717522 | intron variant | A/G;T | snv | 5 | |||
| rs758244932 | 0.827 | 0.120 | 1 | 225828842 | missense variant | C/T | snv | 1.3E-04 | 1.0E-04 | 5 | |
| rs10922106 | 0.925 | 0.080 | 1 | 196722334 | intron variant | A/G | snv | 0.43 | 4 | ||
| rs198388 | 0.851 | 0.160 | 1 | 11857283 | downstream gene variant | C/G;T | snv | 4 | |||
| rs301819 | 0.882 | 0.120 | 1 | 8441726 | intron variant | A/G;T | snv | 4 | |||
| rs71636784 | 1.000 | 0.040 | 1 | 26842709 | intron variant | T/G | snv | 0.12 | 4 | ||
| rs7540032 | 0.925 | 0.080 | 1 | 196732154 | intron variant | C/T | snv | 0.44 | 4 | ||
| rs10429950 | 1.000 | 0.040 | 1 | 218451191 | intergenic variant | T/C | snv | 0.33 | 3 | ||
| rs12759054 | 1.000 | 0.040 | 1 | 233984064 | intron variant | T/A;C | snv | 3 | |||
| rs4846480 | 1.000 | 0.040 | 1 | 218425127 | intron variant | A/T | snv | 0.33 | 3 | ||
| rs7535263 | 0.925 | 0.080 | 1 | 196713216 | intron variant | G/A;C | snv | 3 | |||
| rs10465586 | 1.000 | 0.040 | 1 | 196718199 | intron variant | A/T | snv | 0.44 | 2 |