Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113309773 1.000 0.080 16 75398788 intron variant -/A;C ins 0.51 1
rs11413744 1.000 0.080 4 147474132 intergenic variant -/T delins 0.15 1
rs2876300 1.000 0.080 6 12893871 intron variant A/C;G snv 1
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
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
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs2229116 0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs28362261 0.851 0.160 1 55058129 missense variant A/G snv 1.2E-03 4.8E-03 6
rs17128183 0.882 0.120 14 55112795 intergenic variant A/G snv 0.57 5
rs371237692
REN
0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05 5
rs367650109 1.000 0.080 1 186675959 missense variant A/G snv 4.0E-06 2.1E-05 1
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs879254850 0.776 0.160 19 11113365 missense variant A/G;T snv 4.0E-06 9
rs771479424 0.882 0.120 1 55052764 stop gained A/G;T snv 1.2E-05 3