Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886905373 0.925 0.120 14 94614481 missense variant G/A snv 2.8E-05 3
rs10986769 0.925 0.120 9 125460061 intron variant A/G;T snv 2
rs12679196 0.925 0.120 8 139800104 intron variant C/T snv 0.13 2
rs1324694 0.925 0.120 10 100186688 upstream gene variant C/T snv 7.8E-02 2
rs144757781 0.925 0.120 21 46431895 missense variant G/A;T snv 5.5E-04 2
rs16936752 0.925 0.120 9 93301408 intron variant T/G snv 8.3E-02 2
rs710968 0.925 0.120 7 74083398 intron variant A/G snv 0.75 2
rs762890408 0.925 0.120 21 46431646 missense variant C/T snv 4.0E-05 2.8E-05 2
rs200525645
F2
1.000 0.120 11 46725970 missense variant G/A;T snv 2.0E-05 1
rs3111754 1.000 0.120 2 230868988 intron variant T/C snv 0.43 1
rs73933023 1.000 0.120 19 38566975 missense variant C/G;T snv 2.1E-03 1
rs777785946
F2
1.000 0.120 11 46723267 missense variant G/A snv 7.0E-06 1
rs619203 0.851 0.160 6 117301021 missense variant G/C snv 0.20 0.19 6
rs55951658 0.827 0.200 7 99770202 missense variant T/A;C snv 4.1E-04 9.8E-05 7
rs1800977 0.851 0.240 9 104928169 intron variant G/A;C snv 5
rs121918097
TTR
0.790 0.280 18 31595137 missense variant G/A snv 10
rs1059703 0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs3027898 0.752 0.360 X 154010439 downstream gene variant C/A snv 11
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246