Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 1
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 7
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 4
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 1
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 2
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 2
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 3
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 1
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 1
rs28897672 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 2
rs2070074 0.742 0.360 9 34649445 missense variant A/G snv 9.2E-02 7.4E-02 1
rs387906659 0.742 0.280 19 40257052 stop gained C/A;T snv 1
rs200928781 0.752 0.240 22 28695800 missense variant T/A;C;G snv 2.4E-05 1
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 3
rs55770810 0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 3
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 2
rs41293459 0.763 0.280 17 43063930 missense variant C/A;G;T snv 2.4E-05 1
rs28897696 0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 1
rs748876625 0.807 0.160 17 43104122 missense variant C/A;G snv 1.2E-05 1
rs80357474 0.827 0.200 17 43049188 missense variant A/C;G;T snv 8.0E-06 3