Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
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
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
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
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1800435 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 7