| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs764168570 | 1.000 | 0.120 | 3 | 12608879 | synonymous variant | C/T | snv | 7.0E-06 | 1 | ||
| rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 28 | ||
| rs11943456 | 0.708 | 0.320 | 4 | 55410167 | intron variant | T/C | snv | 0.42 | 18 | ||
| rs3749474 | 0.724 | 0.320 | 4 | 55434518 | 3 prime UTR variant | C/T | snv | 0.33 | 17 | ||
| rs1049216 | 0.790 | 0.200 | 4 | 184628935 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
| rs6449182 | 0.807 | 0.160 | 4 | 15778830 | intron variant | C/G | snv | 0.22 | 6 | ||
| rs4833103 | 0.925 | 0.160 | 4 | 38813881 | intron variant | A/C | snv | 0.64 | 5 | ||
| rs6948 | 1.000 | 0.120 | 4 | 184627976 | 3 prime UTR variant | G/T | snv | 0.48 | 3 | ||
| rs10008492 | 1.000 | 0.120 | 4 | 38764099 | intergenic variant | C/G;T | snv | 2 | |||
| rs4648022 | 1.000 | 0.120 | 4 | 102575280 | intron variant | C/A;T | snv | 1 | |||
| rs1801394 | 0.531 | 0.840 | 5 | 7870860 | missense variant | A/G | snv | 0.47 | 0.45 | 101 | |
| rs351855 | 0.597 | 0.560 | 5 | 177093242 | missense variant | G/A | snv | 0.33 | 0.26 | 58 | |
| rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 52 | |
| rs401681 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 42 | ||
| rs4975616 | 0.763 | 0.320 | 5 | 1315545 | downstream gene variant | G/A | snv | 0.51 | 12 | ||
| rs1494555 | 0.790 | 0.120 | 5 | 35871088 | missense variant | G/A | snv | 0.64 | 0.72 | 8 | |
| rs41291957 | 0.882 | 0.200 | 5 | 149428827 | intron variant | G/A | snv | 0.12 | 7 | ||
| rs1045241 | 1.000 | 0.120 | 5 | 119393591 | 3 prime UTR variant | C/T | snv | 0.30 | 6 | ||
| rs3733846 | 0.807 | 0.200 | 5 | 149425059 | non coding transcript exon variant | T/C | snv | 0.19 | 6 | ||
| rs2069812 | 0.851 | 0.240 | 5 | 132544224 | intron variant | A/G | snv | 0.54 | 5 | ||
| rs147603016 | 0.925 | 0.160 | 5 | 177093286 | synonymous variant | G/A;C | snv | 1.5E-04; 8.2E-06 | 3 | ||
| rs161870 | 0.925 | 0.160 | 5 | 7878079 | synonymous variant | T/C | snv | 0.18 | 0.21 | 2 | |
| rs13178127 | 1.000 | 0.120 | 5 | 83293613 | intron variant | A/G | snv | 3.3E-02 | 1 | ||
| rs146713238 | 1.000 | 0.120 | 5 | 132679861 | missense variant | G/A | snv | 3.2E-05 | 8.4E-05 | 1 | |
| rs17723799 | 1.000 | 0.120 | 5 | 149427514 | non coding transcript exon variant | C/T | snv | 9.9E-02 | 1 |