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
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
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs12713559 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 10