Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs786201059 0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
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
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 10
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
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519985 0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs1057519986 0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519987 0.776 0.280 17 7673810 missense variant A/C snv 9
rs1057519988 0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
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
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs1057520004 0.752 0.240 17 7674884 missense variant A/C;T snv 11
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17