Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs743811 0.882 0.160 22 35396981 upstream gene variant T/A;C snv 4
rs12197043 0.882 0.160 6 149130141 regulatory region variant A/G snv 0.37 3
rs1670754 0.882 0.160 4 32263375 intergenic variant G/A snv 0.24 3
rs4897081 0.882 0.160 6 149115402 upstream gene variant G/A;T snv 3
rs8014363 0.882 0.160 14 53964857 downstream gene variant C/T snv 0.61 3
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs12917114 0.925 0.080 15 47852953 intron variant C/T snv 8.9E-02 2
rs730947 0.925 0.080 2 218838575 upstream gene variant A/C snv 1.0E-01 2
rs77113398 0.925 0.080 13 106451558 intergenic variant G/A snv 6.0E-03 2
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2229109 0.807 0.240 7 87550493 missense variant C/A;T snv 2.7E-02 8
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs10404257 0.925 0.080 19 38645846 upstream gene variant G/A snv 0.50 2
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs7583877 0.925 0.080 2 99844192 intron variant C/T snv 0.61 2
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs121908525 0.790 0.160 2 240875159 missense variant T/C snv 4.4E-05 5.6E-05 7
rs121908529 0.851 0.160 2 240871433 missense variant G/A;C snv 5.6E-04 4