Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12788925 1.000 0.040 11 102931118 intergenic variant A/G snv 0.32 1
rs12999907 1.000 0.040 2 164100741 intron variant A/G snv 0.17 1
rs13088645 1.000 0.040 3 134438421 downstream gene variant T/A;G snv 1
rs13102675 1.000 0.040 4 124978810 intergenic variant T/C snv 0.33 1
rs13144478 0.882 0.040 4 115275150 regulatory region variant A/T snv 5.5E-02 1
rs1321309 1.000 0.040 6 36670859 upstream gene variant G/A;C;T snv 0.38 1
rs1405130 1.000 0.040 2 234655048 intergenic variant T/C snv 0.39 1
rs142695226 1.000 0.040 3 124756354 intergenic variant T/G snv 1
rs145099029 1.000 0.040 6 160871806 downstream gene variant A/C snv 2.6E-03 1
rs145542470 1.000 0.040 9 21953100 intron variant G/A;C;T snv 1.4E-02 1
rs147802096 1.000 0.040 6 36672808 upstream gene variant A/C;T snv 1
rs1508798 1.000 0.040 5 9556582 intergenic variant T/C snv 0.19 1
rs1657346 1.000 0.040 10 44282112 downstream gene variant G/A;C;T snv 1
rs16986953 1.000 0.040 2 19742712 intergenic variant G/A snv 0.11 1
rs17035270 1.000 0.040 4 105115388 intron variant T/C snv 0.20 1
rs17091891 1.000 0.040 8 19985660 intergenic variant T/A;C snv 1
rs17263917 1.000 0.040 5 9552226 downstream gene variant G/A snv 0.11 1
rs1746049 1.000 0.040 10 44280862 downstream gene variant C/T snv 0.23 1
rs17581137 1.000 0.040 15 95603185 intergenic variant A/C;G snv 1
rs17612693 1.000 0.040 4 147444187 intergenic variant T/A snv 0.16 1
rs1807214 1.000 0.040 15 89022026 regulatory region variant A/C snv 0.29 1
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 1
rs2011767 1.000 0.040 17 49262935 intron variant C/A;T snv 1
rs2052923 1.000 0.040 2 43184681 intergenic variant C/T snv 0.61 1
rs2081914 1.000 0.040 5 123337928 intergenic variant C/G;T snv 1