Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11466023 0.827 0.320 16 3249586 missense variant G/A;T snv 1.5E-02; 4.0E-05 6
rs121908513 0.807 0.280 2 32116145 missense variant T/A snv 6
rs864622269 0.851 0.240 14 50628394 missense variant C/T snv 4.0E-06 7.0E-06 6
rs886041761 0.925 0.200 1 110603902 missense variant C/T snv 6
rs104894490 0.827 0.240 15 22812252 missense variant G/A;C snv 5
rs119476046 0.827 0.240 14 50613343 missense variant C/T snv 5
rs2228044 0.882 0.240 5 55968325 missense variant C/G snv 0.13 0.21 5
rs121434441 0.882 0.240 12 57569015 missense variant A/G snv 3
rs121908517 0.925 0.240 2 32063965 missense variant C/A snv 3.9E-04 6.2E-04 3
rs121918262 0.882 0.240 2 86282216 missense variant G/A;T snv 4.0E-06 3
rs483352923 0.882 0.160 5 138441386 missense variant T/A snv 3
rs121908510 0.925 0.240 2 32136898 missense variant G/A snv 2
rs1331505548 0.925 0.200 2 148949891 missense variant A/G snv 2
rs145555213 0.925 0.160 6 5368994 missense variant G/A;T snv 4.0E-06; 4.0E-06 2
rs200154785
APP
0.925 0.240 21 25997362 missense variant T/A snv 2
rs376971794
TFG
0.925 0.160 3 100728760 missense variant G/A snv 6.4E-05 3.5E-05 2
rs483352925 0.925 0.160 5 138444447 missense variant T/A snv 2
rs768560449 1.000 0.160 2 86166521 missense variant A/G snv 8.1E-06 7.0E-06 2
rs80338865 0.925 0.240 8 125061192 missense variant T/C snv 2
rs143129431
TFG
1.000 0.160 3 100748290 missense variant C/G snv 4.0E-06 1
rs757334523 1.000 0.160 19 10829132 missense variant C/T snv 1
rs762630964 1.000 0.160 2 32145007 missense variant G/A snv 4.0E-06 1
rs989357227
TFG
1.000 0.160 3 100713749 missense variant C/T snv 1.6E-05 1
rs9463772 0.925 0.240 6 52246993 non coding transcript exon variant C/A;T snv 3
rs1800897 0.925 0.240 10 100809115 synonymous variant C/T snv 7.4E-02 0.13 2