Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs11739136 0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs1041740 0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs702553 0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3