Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs688 0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246