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