Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750524
PSEN1
1.000 0.080 14 73198095 missense variant A/C snv 2
rs1163242089
PSEN2
1.000 0.080 1 226885673 missense variant C/G;T snv 1
rs1208508997
APP
1.000 0.080 21 26051097 missense variant G/C snv 4.0E-06 1
rs1347757721
PSEN2
1.000 0.080 1 226894058 missense variant G/C snv 7.0E-06 1
rs1426802434
BIN1
1.000 0.080 2 127070588 missense variant A/T snv 4.0E-06 1
rs182024939
MAPT
1.000 0.080 17 46010327 missense variant G/A;T snv 5.2E-06 1
rs367709245
APP
1.000 0.080 21 25891634 intron variant TACTTA/- delins 2.3E-03 1
rs543578531
GRN
1.000 0.080 17 44349703 missense variant C/A;T snv 2.3E-04; 8.0E-06 1
rs63750110
PSEN2
1.000 0.080 1 226895548 missense variant A/C snv 3.6E-05 3.5E-05 1
rs63751072
PSEN1
1.000 0.080 14 73192761 missense variant G/C snv 1
rs63751320
PSEN1
1.000 0.080 14 73192862 missense variant A/C snv 1
rs747363386
PSEN1
1.000 0.080 14 73173669 missense variant A/C;G snv 8.0E-06 1
rs749453173
APP
1.000 0.080 21 25997360 missense variant G/A;C snv 4.0E-06; 4.0E-06 1
rs923630119
TMEM106B
1.000 0.080 7 12215024 missense variant A/T snv 1
rs1191863771
APP
0.925 0.080 21 25911833 missense variant A/G snv 4.0E-06 3
rs143061887
PSEN2
0.925 0.080 1 226881960 missense variant C/T snv 1.6E-05 5.6E-05 3
rs374263073
LAMC2
0.925 0.120 1 183222116 missense variant G/A;T snv 1.2E-05 3
rs63749961
PSEN1
0.925 0.080 14 73192772 missense variant T/G snv 3
rs63750588
PSEN1
0.925 0.080 14 73173687 missense variant T/A snv 3
rs63751019
PSEN1
0.925 0.080 14 73198066 missense variant C/G snv 3
rs771744744
SMUG1
0.925 0.120 12 54182241 missense variant C/T snv 8.0E-06 3
rs1179768627
PSEN1
0.925 0.080 14 73198064 missense variant T/G snv 4.0E-06 2
rs200169735
PSEN2
0.925 0.080 1 226895498 missense variant C/G;T snv 4.0E-06; 2.8E-05 2
rs200347552
APP
0.925 0.080 21 26090000 missense variant G/A snv 1.6E-05 3.5E-05 2
rs200576075
PSEN1
0.925 0.080 14 73171031 missense variant C/T snv 2