Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10488631 | 0.742 | 0.280 | 7 | 128954129 | upstream gene variant | T/C | snv | 9.0E-02 | 7 | ||
rs10806425 | 0.851 | 0.280 | 6 | 90216893 | intron variant | C/A | snv | 0.33 | 5 | ||
rs10903122 | 0.882 | 0.200 | 1 | 24977085 | intergenic variant | A/G | snv | 0.56 | 5 | ||
rs11221332 | 0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv | 5 | |||
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 | ||
rs11712165 | 0.882 | 0.200 | 3 | 119399949 | intron variant | T/G | snv | 0.30 | 5 | ||
rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 5 | |||
rs12928822 | 0.882 | 0.200 | 16 | 11310036 | intron variant | C/T | snv | 0.13 | 5 | ||
rs13003464 | 0.827 | 0.200 | 2 | 60959694 | intron variant | A/G | snv | 0.50 | 7 | ||
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 | |||
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 | |||
rs13315591 | 0.925 | 0.160 | 3 | 58571114 | intron variant | T/C | snv | 0.15 | 4 | ||
rs1464510 | 0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv | 7 | |||
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 | ||
rs17810546 | 0.827 | 0.440 | 3 | 159947262 | intron variant | A/G | snv | 8.2E-02 | 6 | ||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 8 | ||
rs212389 | 0.925 | 0.160 | 6 | 159068759 | non coding transcript exon variant | G/A | snv | 0.60 | 3 | ||
rs2327832 | 0.790 | 0.320 | 6 | 137651931 | intergenic variant | A/G | snv | 0.16 | 6 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 13 | |
rs26232 | 0.925 | 0.160 | 5 | 103261019 | intron variant | C/T | snv | 0.30 | 4 | ||
rs2736340 | 0.683 | 0.480 | 8 | 11486464 | upstream gene variant | C/T | snv | 0.25 | 7 |