Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113795008 | 1.000 | 0.120 | 11 | 192836 | intron variant | A/G | snv | 0.17 | 1 | ||
rs2280540 | 1.000 | 0.120 | 11 | 192997 | intron variant | G/A;C;T | snv | 1 | |||
rs338598 | 1.000 | 0.120 | 19 | 41195623 | intron variant | C/A;G;T | snv | 1 | |||
rs17718444 | 1.000 | 0.120 | 3 | 71450250 | intron variant | C/T | snv | 0.27 | 1 | ||
rs6543124 | 1.000 | 0.120 | 2 | 102370999 | intron variant | T/A | snv | 0.44 | 1 | ||
rs62408225 | 1.000 | 0.120 | 6 | 90246690 | intron variant | A/G | snv | 0.26 | 2 | ||
rs828618 | 0.925 | 0.160 | 3 | 98822789 | intron variant | G/A | snv | 0.28 | 0.22 | 2 | |
rs2427827 | 1.000 | 0.120 | 1 | 159302021 | intron variant | T/C | snv | 0.65 | 2 | ||
rs1391371 | 0.925 | 0.160 | 6 | 32636021 | intron variant | A/C;T | snv | 2 | |||
rs7817 | 0.925 | 0.200 | 7 | 112475603 | 3 prime UTR variant | C/G;T | snv | 2 | |||
rs8046011 | 1.000 | 0.120 | 16 | 11226805 | downstream gene variant | G/A;T | snv | 3 | |||
rs4150407 | 1.000 | 0.120 | 2 | 127292055 | 3 prime UTR variant | T/C | snv | 0.47 | 3 | ||
rs4807542 | 1.000 | 0.120 | 19 | 1104079 | synonymous variant | G/A;C | snv | 0.22; 1.8E-05 | 3 | ||
rs3807213 | 0.882 | 0.200 | 7 | 112465699 | intron variant | G/T | snv | 0.57 | 3 | ||
rs1888909 | 0.882 | 0.200 | 9 | 6197392 | downstream gene variant | T/A;C | snv | 4 | |||
rs10905284 | 0.882 | 0.200 | 10 | 8073399 | intron variant | C/A;T | snv | 4 | |||
rs1444782 | 0.851 | 0.240 | 10 | 9016708 | intergenic variant | G/A | snv | 0.35 | 5 | ||
rs28383314 | 0.925 | 0.160 | 6 | 32619436 | regulatory region variant | T/C | snv | 0.61 | 5 | ||
rs74767530 | 0.851 | 0.320 | 7 | 117627537 | stop gained | C/T | snv | 5.6E-05 | 4.9E-05 | 5 | |
rs2428494 | 0.827 | 0.160 | 6 | 31354420 | intron variant | T/A;C | snv | 5 | |||
rs9268644 | 0.827 | 0.360 | 6 | 32440267 | intron variant | A/C | snv | 0.68 | 5 | ||
rs7302200 | 0.851 | 0.200 | 12 | 56055651 | regulatory region variant | G/A | snv | 0.23 | 6 | ||
rs3129878 | 0.807 | 0.360 | 6 | 32440958 | intron variant | A/C | snv | 0.30 | 6 | ||
rs34210653 | 0.807 | 0.280 | 17 | 4632019 | missense variant | G/A | snv | 2.7E-02 | 1.7E-02 | 8 | |
rs1420101 | 0.827 | 0.280 | 2 | 102341256 | synonymous variant | C/T | snv | 0.33 | 0.35 | 8 |