Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786203071 0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs786201419 0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
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
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15