Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 64
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs1475170339 0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1800014 0.776 0.200 20 4699875 missense variant G/A snv 8.0E-03 2.2E-03 11
rs141138948 0.807 0.120 9 37783993 missense variant T/C;G snv 4.1E-04 9
rs62643364 0.851 0.160 20 4699466 synonymous variant A/G;T snv 4.0E-06; 1.4E-04 7
rs1064039 0.827 0.200 20 23637790 missense variant C/G;T snv 0.20 6
rs121908345 0.827 0.240 22 50080391 missense variant G/A snv 1.3E-04 6.3E-05 6
rs28939711 0.851 0.120 10 99724057 missense variant G/A snv 3.2E-05 3.5E-05 5
rs587777162 0.925 0.040 20 63495972 missense variant C/T snv 5
rs1364050643 0.851 0.240 2 86232711 missense variant G/A snv 5
rs1051169 0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 5
rs267607102 0.851 0.120 1 11022196 missense variant A/G snv 5
rs80356717 0.851 0.120 1 11018836 missense variant A/G snv 5
rs397514662 0.882 0.120 10 99716419 missense variant A/C;G snv 1.2E-05 4
rs121434444 0.882 0.160 12 57569648 missense variant C/T snv 2.8E-05 7.0E-06 4
rs398122370 0.925 0.160 20 4699851 missense variant G/C snv 4