Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3764261 | 0.732 | 0.280 | 16 | 56959412 | upstream gene variant | C/A | snv | 0.31 | 26 | ||
rs562338 | 0.807 | 0.160 | 2 | 21065449 | intergenic variant | A/G | snv | 0.69 | 21 | ||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 19 | ||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 16 | |||
rs17321515 | 0.776 | 0.200 | 8 | 125474167 | intron variant | A/G | snv | 0.49 | 16 | ||
rs2943634 | 0.763 | 0.200 | 2 | 226203364 | intergenic variant | A/C;G | snv | 15 | |||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs9989419 | 0.882 | 0.120 | 16 | 56951227 | regulatory region variant | A/G | snv | 0.55 | 11 | ||
rs3865188 | 0.790 | 0.320 | 16 | 82617112 | intergenic variant | A/G;T | snv | 10 | |||
rs501120 | 0.763 | 0.240 | 10 | 44258419 | downstream gene variant | T/C | snv | 0.24 | 10 | ||
rs6834314 | 0.807 | 0.160 | 4 | 87292656 | intergenic variant | A/G | snv | 0.24 | 10 | ||
rs10759931 | 0.790 | 0.360 | 9 | 117701869 | upstream gene variant | G/A;T | snv | 9 | |||
rs6905288 | 0.882 | 0.120 | 6 | 43791136 | downstream gene variant | G/A | snv | 0.56 | 9 | ||
rs17482753 | 1.000 | 0.080 | 8 | 19975135 | regulatory region variant | G/T | snv | 8.8E-02 | 8 | ||
rs1154988 | 3 | 136206349 | upstream gene variant | T/A | snv | 0.76 | 7 | ||||
rs17411031 | 0.925 | 0.120 | 8 | 19994799 | regulatory region variant | C/G | snv | 0.25 | 7 | ||
rs267734 | 0.925 | 0.120 | 1 | 150979001 | upstream gene variant | T/C | snv | 0.14 | 7 | ||
rs11084753 | 1.000 | 0.080 | 19 | 33831232 | intergenic variant | A/C;G;T | snv | 0.65 | 6 | ||
rs13125101 | 4 | 80253438 | TF binding site variant | G/A | snv | 0.24 | 6 | ||||
rs1887320 | 20 | 10985350 | intron variant | G/A | snv | 0.46 | 6 | ||||
rs2643826 | 3 | 27521497 | upstream gene variant | C/T | snv | 0.56 | 6 | ||||
rs10059884 | 5 | 32832368 | regulatory region variant | C/A;T | snv | 5 | |||||
rs2823139 | 1.000 | 0.080 | 21 | 15204463 | intron variant | G/A | snv | 0.34 | 5 | ||
rs17477177 | 1.000 | 0.080 | 7 | 106771412 | upstream gene variant | T/C | snv | 0.17 | 4 | ||
rs2770150 | 0.925 | 0.080 | 9 | 117700861 | upstream gene variant | A/G | snv | 0.22 | 4 |