Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 8
rs17694933 1.000 0.040 9 22164310 intergenic variant G/A snv 0.50 3
rs1800907 0.925 0.120 7 142800425 upstream gene variant T/C snv 0.56 3
rs62355900 1.000 0.040 5 56756868 regulatory region variant T/C snv 0.15 3
rs7041895 1.000 0.040 9 22162795 intergenic variant A/C snv 0.47 3
rs10859871 1.000 0.040 12 95318100 intron variant A/C snv 0.37 2
rs12030576 1.000 0.040 1 115274600 intron variant G/C;T snv 2
rs12455952 1.000 0.040 18 61173285 intergenic variant T/C;G snv 0.19 2
rs12700667 0.925 0.080 7 25862019 intergenic variant G/A snv 0.63 2
rs80111889 1.000 0.040 2 112809853 intergenic variant T/G snv 0.26 2
rs10131751 1.000 0.040 14 28212010 intergenic variant C/A snv 9.2E-02 1
rs10167914 1.000 0.040 2 112805784 TF binding site variant A/G snv 0.31 1
rs10508881 1.000 0.040 10 44046117 regulatory region variant A/G snv 0.50 1
rs113850637 1.000 0.040 3 104131556 intergenic variant C/T snv 0.14 1
rs1432089 1.000 0.040 4 170869637 intergenic variant C/T snv 0.37 1
rs1448792 1.000 0.040 9 22641634 upstream gene variant A/G snv 0.71 1
rs1537377 1.000 0.040 9 22169701 regulatory region variant T/C snv 0.44 1
rs1903068 1.000 0.040 4 55142310 intergenic variant A/G snv 0.25 1
rs1995051 1.000 0.040 7 45885442 upstream gene variant A/G snv 0.70 1
rs2738113 1.000 0.040 8 6971563 upstream gene variant G/A;T snv 1
rs4654783 1.000 0.040 1 22113027 downstream gene variant T/C snv 0.70 1
rs60966186 1.000 0.040 8 6973682 upstream gene variant A/G snv 1
rs6542095 1.000 0.040 2 112771606 downstream gene variant C/A;T snv 1
rs6757804 1.000 0.040 2 150779318 regulatory region variant C/T snv 0.58 1
rs71415016 1.000 0.040 14 95977621 intergenic variant T/C snv 6.1E-02 1