Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
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
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 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
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs6927172 0.851 0.120 6 137681038 intron variant C/A;G;T snv 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
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 4
rs17144046 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 4
rs1999071 0.851 0.080 14 22659998 regulatory region variant T/C snv 0.29 4
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 4
rs9901146 0.882 0.160 17 39887090 intergenic variant G/A snv 0.45 4
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4
rs10036789 1.000 0.080 5 72400091 regulatory region variant C/A;G snv 3
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3