Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs11650680 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 5
rs117710327 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 5
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs62322662 0.925 0.080 4 122438414 intergenic variant A/G snv 5.1E-02 4
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs1775554 0.882 0.080 10 9012377 intergenic variant A/C snv 0.35 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3
rs10795672 0.925 0.080 10 8735677 intergenic variant G/A;T snv 2
rs11742240 0.925 0.080 5 35881274 downstream gene variant G/A;T snv 2
rs190438685 0.925 0.080 4 39388825 intergenic variant C/T snv 6.2E-03 2
rs2381712 0.925 0.080 2 145387450 intergenic variant T/G snv 0.52 2
rs28415845 0.925 0.080 11 1151933 regulatory region variant T/C snv 0.58 2
rs35204956 0.925 0.080 8 80389778 intron variant A/-;AA;AAA delins 2
rs4771332 0.925 0.080 13 99418203 upstream gene variant T/A;C;G snv 2
rs540485182 0.925 0.080 5 110825774 intergenic variant -/A;AA;AAA delins 2
rs60227565 0.925 0.080 2 102275879 intergenic variant G/A;T snv 0.10 2
rs62557312 0.925 0.080 9 6047765 intron variant C/T snv 0.15 2
rs7099257 0.925 0.080 10 8468994 upstream gene variant T/A snv 0.49 2
rs12617922 1.000 2 145399111 intergenic variant G/A snv 0.46 1