Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs1057519732 0.827 0.160 15 66436824 missense variant C/A;T snv 6
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519841 0.925 0.120 5 68295269 missense variant A/G snv 5
rs1057519874 0.807 0.120 7 6387261 missense variant C/A;T snv 4
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057519890 0.807 0.200 17 39723966 missense variant T/A snv 7
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519917 0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 9
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
rs1057519948 0.851 0.120 7 6387262 missense variant C/T snv 4
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 12
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37