Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs769665945 0.882 0.160 7 101137079 missense variant C/A;T snv 4.0E-06; 3.6E-05 3
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs4485213 1.000 0.120 13 105256524 intergenic variant C/T snv 0.19 1
rs951660 1.000 0.120 3 111919285 intron variant A/C snv 0.86 1
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs117834366 0.925 0.120 7 147937799 intron variant G/A snv 1.2E-02 2
rs17501010 0.827 0.320 3 190308865 intron variant G/T snv 0.15 5
rs893051 0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs3813034 0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs140701 0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs4795541 0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1799990 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs944050 0.827 0.280 14 64233327 splice region variant T/C snv 9.5E-02 7.9E-02 5
rs2497931 1.000 0.120 X 67436434 intergenic variant A/C;T snv 1