Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10759931 | 0.790 | 0.360 | 9 | 117701869 | upstream gene variant | G/A;T | snv | 9 | |||
rs10995271 | 0.776 | 0.280 | 10 | 62678726 | downstream gene variant | G/C | snv | 0.32 | 8 | ||
rs2737190 | 0.827 | 0.120 | 9 | 117701903 | upstream gene variant | G/A | snv | 0.52 | 6 | ||
rs7194886 | 0.851 | 0.080 | 16 | 50691282 | upstream gene variant | C/T | snv | 0.38 | 4 | ||
rs4331426 | 0.925 | 0.080 | 18 | 22610832 | intergenic variant | G/A | snv | 0.86 | 2 | ||
rs4788172 | 0.925 | 0.120 | 16 | 29656932 | regulatory region variant | G/A | snv | 0.12 | 2 | ||
rs1568952 | 1.000 | 0.080 | 8 | 58799804 | intergenic variant | T/C | snv | 0.75 | 1 | ||
rs6507226 | 1.000 | 0.080 | 18 | 22611328 | intergenic variant | A/G | snv | 0.45 | 1 | ||
rs9271300 | 1.000 | 0.080 | 6 | 32613805 | intergenic variant | C/G | snv | 0.54 | 1 | ||
rs1042713 | 0.576 | 0.800 | 5 | 148826877 | missense variant | G/A | snv | 0.42 | 0.43 | 63 | |
rs1042714 | 0.597 | 0.640 | 5 | 148826910 | stop gained | G/C;T | snv | 0.68 | 54 | ||
rs1800870 | 0.851 | 0.200 | 17 | 19649164 | intron variant | C/T | snv | 5 | |||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 121 | |
rs2072069 | 0.925 | 0.120 | 17 | 34357972 | intron variant | G/A | snv | 0.47 | 2 | ||
rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 68 | |
rs4804803 | 0.732 | 0.360 | 19 | 7747847 | upstream gene variant | A/G | snv | 0.26 | 15 | ||
rs373950030 | 0.882 | 0.080 | 19 | 7744967 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 3 | |
rs3211956 | 0.925 | 0.160 | 7 | 80674446 | intron variant | T/G | snv | 6.7E-02 | 3 | ||
rs10499859 | 0.925 | 0.120 | 7 | 80629494 | intron variant | A/G | snv | 0.46 | 2 | ||
rs1194182 | 1.000 | 0.080 | 7 | 80602188 | 5 prime UTR variant | G/C | snv | 0.53 | 2 | ||
rs3092923 | 1.000 | 0.080 | X | 136659026 | intron variant | T/C | snv | 0.17 | 0.28 | 1 | |
rs6768300 | 0.925 | 0.120 | 3 | 50611939 | 5 prime UTR variant | C/G | snv | 0.85 | 2 | ||
rs10841845 | 0.925 | 0.200 | 12 | 8533837 | 3 prime UTR variant | A/G | snv | 0.28 | 2 | ||
rs10841847 | 1.000 | 0.080 | 12 | 8535216 | intron variant | A/G | snv | 0.58 | 1 | ||
rs34069356 | 0.925 | 0.080 | 20 | 58995705 | missense variant | C/T | snv | 1.1E-03 | 4.3E-03 | 2 |