Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2047076 | 5 | 76762684 | intergenic variant | C/T | snv | 0.14 | 2 | ||||
rs2485713 | 10 | 8423240 | intron variant | G/C;T | snv | 2 | |||||
rs2521295 | 11 | 2327630 | downstream gene variant | T/A;C | snv | 2 | |||||
rs2523552 | 6 | 31364177 | upstream gene variant | C/T | snv | 0.15 | 2 | ||||
rs2732716 | 17 | 46245680 | downstream gene variant | T/A;C | snv | 2 | |||||
rs2734037 | 3 | 128590041 | intergenic variant | C/T | snv | 0.34 | 2 | ||||
rs2817441 | 6 | 156617565 | regulatory region variant | C/T | snv | 0.26 | 2 | ||||
rs3095254 | 6 | 31253891 | intergenic variant | C/A;G | snv | 0.55 | 2 | ||||
rs34018670 | 16 | 80809337 | upstream gene variant | -/AG | delins | 0.17 | 2 | ||||
rs35110517 | 7 | 28267686 | intergenic variant | T/G | snv | 0.20 | 2 | ||||
rs4020660 | 12 | 6402491 | intergenic variant | G/A;T | snv | 2 | |||||
rs434216 | 16 | 85893407 | regulatory region variant | T/A;C | snv | 2 | |||||
rs4385425 | 7 | 50267738 | upstream gene variant | A/G | snv | 0.40 | 2 | ||||
rs4566648 | 4 | 83238066 | intron variant | T/G | snv | 0.47 | 2 | ||||
rs4811020 | 20 | 50286497 | downstream gene variant | C/T | snv | 0.29 | 2 | ||||
rs4843869 | 16 | 85941535 | intron variant | G/A | snv | 0.18 | 2 | ||||
rs4919087 | 10 | 97312750 | upstream gene variant | A/G;T | snv | 2 | |||||
rs531425523 | 22 | 17354388 | upstream gene variant | T/C | snv | 8.4E-05 | 2 | ||||
rs55793580 | 9 | 124247116 | regulatory region variant | C/T | snv | 0.16 | 2 | ||||
rs562398803 | 20 | 50492033 | regulatory region variant | AA/-;A;AAA;AAAA;AAAAA | delins | 2 | |||||
rs58681483 | 17 | 59857293 | downstream gene variant | A/G | snv | 0.13 | 2 | ||||
rs5875374 | 6 | 32459228 | downstream gene variant | -/AC | delins | 0.72 | 2 | ||||
rs58904263 | 20 | 31813603 | upstream gene variant | -/G | ins | 2 | |||||
rs62191825 | 2 | 219187607 | downstream gene variant | T/C | snv | 3.6E-02 | 2 | ||||
rs62242983 | 3 | 46342431 | intergenic variant | T/A;C | snv | 0.14 | 2 |