Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1256046734 0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 12
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1289543302 0.763 0.440 7 87536472 missense variant C/T snv 12
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1800234 0.807 0.240 22 46219983 missense variant T/A;C snv 4.0E-06; 1.1E-02 6
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101