Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77294580
ACE
1.000 0.040 17 63480396 missense variant G/A;T snv 4.0E-06; 4.0E-06 1
rs782591769
ELN
1.000 0.040 7 74045237 missense variant G/C snv 8.0E-06 1
rs8125581 1.000 0.040 20 46010604 missense variant G/A snv 3.0E-04 3.4E-04 1
rs9316871 1.000 0.040 13 22287782 intergenic variant A/G snv 0.22 1
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs595244 0.882 0.080 15 48548638 intron variant C/T snv 7.7E-02 3
rs764522 0.882 0.080 3 30605058 upstream gene variant G/A;C snv 3
rs7866503 0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs8087799 0.882 0.080 18 22605468 regulatory region variant G/A snv 0.43 3
rs919433 0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs201191171 0.925 0.080 20 46013279 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 2
rs326118 0.925 0.080 5 7868430 intron variant T/G snv 0.21 2
rs773474756 0.925 0.080 11 102790467 missense variant T/C snv 8.1E-06 2
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs5516 0.827 0.120 19 50820217 missense variant C/G snv 0.69 0.67 6
rs1057335 0.827 0.120 17 1754359 missense variant G/A snv 0.22 0.20 5
rs12191786 0.851 0.120 6 22004398 intron variant C/A;T snv 4
rs486055 0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 3
rs3019885 0.925 0.120 8 117013406 intron variant T/A;G snv 2
rs4988300 0.925 0.120 11 68321363 intron variant G/T snv 0.50 2
rs1466535 0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs3877899 0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 7
rs12692386 0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs1524668 0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs8003379 0.882 0.160 14 64406881 intron variant A/C snv 0.23 3