Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs4594881 1.000 0.080 5 35846713 intergenic variant G/T snv 0.28 2
rs7936312 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 5
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs2814778 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 24
rs9807989 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 2
rs3024971 0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7