Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs4773144 0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs4845625 0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7901695 0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9319428 0.925 0.080 13 28399484 intron variant G/A snv 0.30 4
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
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
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82