Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
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
rs149680468 0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12