Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2069840 0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs281432 0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs743507 0.882 0.200 7 151010400 intron variant C/T snv 0.77 4
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
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
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1926447 0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11