Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs3825172 0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs74421874 0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs1800012 0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs12722 0.882 0.120 9 134842570 3 prime UTR variant C/T snv 0.44 6
rs370579379 0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 6
rs121918082
TTR
0.827 0.280 18 31595244 missense variant G/C snv 6
rs958191819
TTR
0.851 0.240 18 31595212 missense variant A/T snv 7.0E-06 6
rs72755233 1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs62621197 1.000 0.080 19 8605262 missense variant C/A;T snv 4.1E-06; 3.1E-02 2.9E-02 4
rs121918088
TTR
0.851 0.120 18 31598631 missense variant T/C snv 4
rs486055 0.925 0.120 11 102779693 missense variant C/G;T snv 1.2E-05; 0.10 3
rs267607247
MPZ
0.882 0.120 1 161305953 missense variant C/A snv 3
rs121918091
TTR
0.882 0.200 18 31595169 missense variant T/C snv 4.0E-06 3
rs1863190 1.000 0.080 2 217263429 non coding transcript exon variant A/T snv 0.53 2
rs13113 0.925 0.200 2 201287439 3 prime UTR variant T/A snv 0.33 2