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
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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
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
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs5355 0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs5351 0.807 0.240 13 77901178 synonymous variant T/C;G snv 0.57 7