Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1746048 | 0.776 | 0.120 | 10 | 44280376 | downstream gene variant | C/T | snv | 0.25 | 8 | ||
rs1867624 | 0.851 | 0.080 | 17 | 64309731 | upstream gene variant | C/T | snv | 0.65 | 4 | ||
rs1878406 | 0.807 | 0.200 | 4 | 147472512 | intergenic variant | C/A;G;T | snv | 7 | |||
rs2107595 | 0.732 | 0.280 | 7 | 19009765 | regulatory region variant | G/A | snv | 0.19 | 15 | ||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 15 | |||
rs2943641 | 0.763 | 0.160 | 2 | 226229029 | intergenic variant | T/C | snv | 0.67 | 18 | ||
rs2943650 | 0.827 | 0.120 | 2 | 226241205 | intergenic variant | C/T | snv | 0.58 | 6 | ||
rs2972146 | 0.882 | 0.040 | 2 | 226235982 | intergenic variant | G/T | snv | 0.72 | 9 | ||
rs3939286 | 0.776 | 0.360 | 9 | 6210099 | regulatory region variant | T/A;C | snv | 12 | |||
rs4552883 | 0.925 | 0.040 | 8 | 139234730 | regulatory region variant | G/A;C | snv | 2 | |||
rs501120 | 0.763 | 0.240 | 10 | 44258419 | downstream gene variant | T/C | snv | 0.24 | 10 | ||
rs7833904 | 0.882 | 0.040 | 8 | 58505103 | upstream gene variant | A/T | snv | 0.55 | 3 | ||
rs8042271 | 0.882 | 0.040 | 15 | 89030987 | intergenic variant | G/A;T | snv | 3 | |||
rs974819 | 0.807 | 0.080 | 11 | 103789839 | intron variant | T/A;C | snv | 6 | |||
rs2066714 | 0.742 | 0.240 | 9 | 104824472 | missense variant | T/C | snv | 0.21 | 0.25 | 13 | |
rs2066715 | 0.807 | 0.160 | 9 | 104825752 | missense variant | C/T | snv | 8.2E-02 | 5.5E-02 | 7 | |
rs2230806 | 0.689 | 0.280 | 9 | 104858586 | missense variant | C/T | snv | 0.32 | 0.39 | 24 | |
rs28937313 | 0.882 | 0.160 | 9 | 104822520 | missense variant | T/C | snv | 8.0E-06 | 3 | ||
rs4149313 | 0.763 | 0.240 | 9 | 104824472 | missense variant | T/C | snv | 9 | |||
rs57137919 | 0.776 | 0.160 | 21 | 42218908 | intron variant | G/A | snv | 0.14 | 9 | ||
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs4862423 | 0.882 | 0.080 | 4 | 184805394 | intron variant | C/T | snv | 0.37 | 4 | ||
rs3825807 | 0.807 | 0.120 | 15 | 78796769 | missense variant | A/G | snv | 0.34 | 0.33 | 10 | |
rs6918289 | 0.925 | 0.040 | 6 | 41134089 | intron variant | G/T | snv | 9.8E-02 | 2 | ||
rs4961 | 0.683 | 0.400 | 4 | 2904980 | missense variant | G/A;T | snv | 1.2E-05; 0.20 | 27 |