Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3783347 | 14 | 100372924 | intron variant | G/T | snv | 0.16 | 2 | ||||
rs16913693 | 9 | 108918079 | intron variant | T/G | snv | 8.4E-02 | 2 | ||||
rs118137427 | 10 | 111217250 | intergenic variant | A/G | snv | 3.3E-02 | 2 | ||||
rs11195502 | 10 | 111279909 | intergenic variant | C/A;G;T | snv | 2 | |||||
rs10885122 | 1.000 | 0.080 | 10 | 111282335 | intergenic variant | T/G | snv | 0.71 | 4 | ||
rs4506565 | 0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv | 22 | |||
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs12255372 | 0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv | 28 | |||
rs3802177 | 1.000 | 0.080 | 8 | 117172786 | 3 prime UTR variant | G/A | snv | 0.24 | 5 | ||
rs11558471 | 1.000 | 0.080 | 8 | 117173494 | 3 prime UTR variant | A/G | snv | 0.25 | 5 | ||
rs35859536 | 8 | 117179236 | downstream gene variant | C/T | snv | 0.25 | 2 | ||||
rs11257655 | 1.000 | 0.080 | 10 | 12265895 | TF binding site variant | C/T | snv | 0.23 | 4 | ||
rs11708067 | 0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 | 9 | ||
rs11717195 | 1.000 | 0.080 | 3 | 123363551 | intron variant | T/C | snv | 0.19 | 3 | ||
rs2877716 | 3 | 123375604 | intron variant | T/C | snv | 0.76 | 4 | ||||
rs10747083 | 12 | 132465032 | downstream gene variant | G/A;T | snv | 2 | |||||
rs3829109 | 9 | 136362314 | intron variant | G/A | snv | 0.25 | 2 | ||||
rs17168486 | 1.000 | 0.080 | 7 | 14858657 | intron variant | C/T | snv | 0.18 | 5 | ||
rs10228456 | 1.000 | 0.080 | 7 | 15024301 | intergenic variant | C/T | snv | 0.54 | 3 | ||
rs2191349 | 1.000 | 0.080 | 7 | 15024684 | intergenic variant | G/T | snv | 0.54 | 4 | ||
rs12055786 | 6 | 153109990 | intron variant | C/T | snv | 0.46 | 3 | ||||
rs2390732 | 2 | 168749457 | intron variant | G/A | snv | 0.65 | 2 | ||||
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 18 | |
rs853789 | 2 | 168944978 | intron variant | A/G;T | snv | 0.75 | 4 | ||||
rs1280 | 3 | 170995501 | intron variant | T/C | snv | 0.20 | 2 |