Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63749836
PSEN1
0.827 0.160 14 73192786 missense variant G/A snv 5
rs63750053
PSEN1
0.827 0.120 14 73192721 missense variant G/T snv 5
rs63750635
MAPT
0.851 0.120 17 46014286 missense variant C/T snv 5
rs1189501362
GSK3B
0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06 4
rs1205185774
AHSA1
0.882 0.120 14 77469161 missense variant C/T snv 4
rs1235948930
MAPT
0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 4
rs1566650594
PSEN1
0.851 0.120 14 73206384 splice acceptor variant A/T snv 4
rs63750450
PSEN1
0.851 0.120 14 73173571 missense variant A/G snv 4
rs866604606
MAPK1
0.882 0.120 22 21772907 missense variant G/A snv 4
rs1182182524
MAPT
0.882 0.120 17 45983724 missense variant T/G snv 1.4E-05 3
rs1595014 0.882 0.120 7 12148903 intergenic variant T/A snv 0.23 3
rs63750487
PSEN1
0.882 0.120 14 73192771 missense variant C/T snv 3
rs63750573
MAPT
0.882 0.120 17 46018627 missense variant A/G snv 3
rs63750905
MAPT
0.882 0.120 17 46018624 missense variant G/T snv 3
rs63751165
MAPT
0.925 0.120 17 46010401 missense variant G/A;T snv 3
rs1295855402
MAPT
0.925 0.120 17 46024034 missense variant C/T snv 7.0E-06 2
rs1804469
MSMB ; LOC105378287
0.925 0.120 10 46033495 missense variant T/C snv 2
rs63750711
MAPT
0.925 0.120 17 46018645 missense variant A/T snv 2
rs63751264
MAPT
0.925 0.120 17 46018726 missense variant A/T snv 2
rs661
PSEN1
0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 6
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs1012826460
MAPT
0.925 0.120 17 45971888 missense variant G/A snv 4.0E-06 1.4E-05 2
rs80356726
TARDBP
0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12