Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs779569800 1.000 0.080 19 44908714 missense variant G/A;C;T snv 1.3E-05; 6.3E-06; 6.3E-06 1
rs1307925400
APP
1.000 0.080 21 26112001 missense variant C/G;T snv 4.0E-06 1
rs1347585131
APP
1.000 0.080 21 26021974 missense variant T/C snv 4.0E-06 1
rs1459435816
APP
1.000 0.080 21 26053249 missense variant G/A snv 4.0E-06 1
rs200487832
APP
1.000 0.080 21 25976000 missense variant C/G;T snv 8.0E-06 7.0E-06 1
rs557227002
APP
1.000 0.080 21 26000158 missense variant G/A snv 2.0E-04 4.9E-05 1
rs63750363
APP
1.000 0.080 21 25897642 missense variant C/G snv 1.2E-05 7.0E-06 1
rs769757835
APP
1.000 0.080 21 26000117 missense variant C/T snv 4.0E-06 1
rs779407819
APP
1.000 0.080 21 26021899 missense variant G/A snv 1.6E-05 1
rs958576773 1.000 0.080 6 33662534 missense variant G/A snv 1
rs1712572 1.000 0.080 3 106898231 non coding transcript exon variant A/C;G;T snv 1
rs1348800465 1.000 0.080 17 45991491 missense variant C/G;T snv 4.0E-06; 4.0E-06 1
rs1015909000 1.000 0.080 9 14146790 missense variant A/G snv 1
rs201617677 1.000 0.080 14 73173698 missense variant G/A;T snv 6.4E-05 1
rs1215971988 1.000 0.080 1 226885618 missense variant T/C snv 4.0E-06 7.0E-06 1
rs1482790603 1.000 0.080 1 226891284 missense variant T/C snv 1.2E-05 7.0E-06 1
rs202178897 1.000 0.080 1 226885596 missense variant G/A;T snv 1.2E-04; 4.0E-06 1
rs1393704451 1.000 0.080 2 109129746 missense variant A/G snv 1
rs139155954 1.000 0.080 4 185662115 missense variant C/G;T snv 6.0E-05 1
rs773029808 1.000 0.080 4 185626897 missense variant C/G snv 2.0E-05 1
rs1220355764
APP
0.925 0.080 21 26022037 missense variant T/C snv 2
rs1302192564
APP
0.925 0.080 21 26000164 missense variant G/A snv 2
rs1451944248
APP
0.925 0.080 21 25975964 missense variant G/A snv 2
rs372642708
APP
0.925 0.080 21 26051152 missense variant C/T snv 2.4E-05 9.8E-05 2
rs372702043
APP
0.925 0.120 21 25976006 missense variant G/A snv 4.0E-06 2.8E-05 2