Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 12
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 12
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913370 0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs869025608 0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs121913369 0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 8
rs121913378 0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs727504317 0.807 0.320 15 66435145 missense variant G/A snv 6
rs1057519729 0.827 0.080 15 66435113 missense variant A/C snv 2