Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28929474 | 0.708 | 0.320 | 14 | 94378610 | missense variant | C/G;T | snv | 2.8E-05; 1.1E-02 | 17 | ||
rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 13 | ||
rs3791679 | 0.925 | 0.120 | 2 | 55869757 | intron variant | A/G | snv | 0.20 | 8 | ||
rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 7 | |||||
rs2812208 | 13 | 50132951 | intron variant | G/A;C | snv | 5 | |||||
rs6918725 | 6 | 126669246 | intron variant | T/G | snv | 0.50 | 4 | ||||
rs12198986 | 6 | 7719826 | regulatory region variant | G/A | snv | 0.37 | 3 | ||||
rs1890995 | 1 | 218431336 | intron variant | G/A | snv | 0.33 | 3 | ||||
rs7155279 | 14 | 92019537 | intron variant | G/A;T | snv | 3 | |||||
rs7753012 | 6 | 142424746 | intron variant | T/G | snv | 0.50 | 3 |