Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
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
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs56062135 0.790 0.200 15 67163292 intron variant C/T snv 0.18 8
rs928413 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs1898671 0.851 0.160 5 111072304 intron variant C/T snv 0.25 5
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs12470864 0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4
rs72823641 0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 4