Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs375752214 0.708 0.400 7 150998541 missense variant C/T snv 4.1E-06 4.2E-05 22
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2268388 0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs4821480 0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93