Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs786201059 0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 20