Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048709 0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs1549758 0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4636297 0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1136287 0.790 0.280 17 1769982 missense variant C/T snv 0.61 0.69 8
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2073618 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs228648 0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs2230774 0.807 0.240 2 11218994 missense variant G/C;T snv 0.49 12
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs17058639 0.925 0.160 3 57896874 splice region variant C/T snv 0.30 0.24 2
rs2000813 0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23 9
rs10490924 0.716 0.240 10 122454932 missense variant G/T snv 0.26 0.23 16
rs6128 0.851 0.360 1 169593666 synonymous variant C/A;T snv 2.8E-05; 0.24 5