Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12928822 | 0.882 | 0.200 | 16 | 11310036 | intron variant | C/T | snv | 0.13 | 5 | ||
rs13010713 | 0.882 | 0.200 | 2 | 181131318 | intron variant | A/C;G | snv | 5 | |||
rs13098911 | 0.882 | 0.200 | 3 | 46193709 | intron variant | C/G;T | snv | 5 | |||
rs13119723 | 0.807 | 0.280 | 4 | 122297158 | intron variant | A/G | snv | 0.10 | 5 | ||
rs13151961 | 0.827 | 0.200 | 4 | 122194347 | intron variant | A/G | snv | 0.11 | 5 | ||
rs13314993 | 0.882 | 0.200 | 3 | 32973977 | regulatory region variant | G/C;T | snv | 5 | |||
rs17035378 | 0.882 | 0.200 | 2 | 68371823 | intron variant | T/A;C | snv | 5 | |||
rs1738074 | 0.790 | 0.320 | 6 | 159044945 | 5 prime UTR variant | T/C | snv | 0.49 | 5 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs2076530 | 0.724 | 0.640 | 6 | 32396039 | missense variant | T/C | snv | 0.42 | 0.40 | 5 | |
rs2298428 | 0.807 | 0.240 | 22 | 21628603 | missense variant | C/T | snv | 0.27 | 0.18 | 5 | |
rs2816316 | 0.882 | 0.200 | 1 | 192567683 | intron variant | C/A | snv | 0.79 | 5 | ||
rs296547 | 0.882 | 0.200 | 1 | 200923009 | intron variant | T/C | snv | 0.53 | 5 | ||
rs4675374 | 0.882 | 0.200 | 2 | 203937855 | intron variant | T/C | snv | 0.65 | 5 | ||
rs4819388 | 0.790 | 0.240 | 21 | 44227538 | 3 prime UTR variant | T/C | snv | 5 | |||
rs5754217 | 0.925 | 0.120 | 22 | 21585386 | intron variant | G/T | snv | 0.31 | 5 | ||
rs6822844 | 0.689 | 0.520 | 4 | 122588266 | regulatory region variant | G/T | snv | 0.10 | 5 | ||
rs802734 | 0.827 | 0.280 | 6 | 127957653 | intergenic variant | A/G;T | snv | 5 | |||
rs9792269 | 0.882 | 0.200 | 8 | 128252343 | intergenic variant | A/C;G | snv | 5 | |||
rs10892258 | 0.925 | 0.120 | 11 | 118709156 | intron variant | G/A | snv | 0.19 | 4 | ||
rs11586238 | 0.925 | 0.160 | 1 | 116720516 | regulatory region variant | C/G | snv | 0.19 | 4 | ||
rs11676922 | 0.925 | 0.160 | 2 | 100190478 | intron variant | T/A | snv | 0.51 | 4 | ||
rs13315591 | 0.925 | 0.160 | 3 | 58571114 | intron variant | T/C | snv | 0.15 | 4 | ||
rs1378942 | 0.790 | 0.240 | 15 | 74785026 | intron variant | C/A;T | snv | 4 | |||
rs1990760 | 0.672 | 0.480 | 2 | 162267541 | missense variant | C/T | snv | 0.50 | 0.45 | 4 |