Disease: Pick Disease of the Brain
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750487
PSEN1
0.882 0.120 14 73192771 missense variant C/T snv 3
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs63750573
MAPT
0.882 0.120 17 46018627 missense variant A/G snv 3
rs63750590
PSEN1
0.790 0.120 14 73186860 missense variant A/G snv 10
rs63750635
MAPT
0.851 0.120 17 46014286 missense variant C/T snv 5
rs63750711
MAPT
0.925 0.120 17 46018645 missense variant A/T snv 2
rs63750905
MAPT
0.882 0.120 17 46018624 missense variant G/T snv 3
rs63751068
PSEN1
0.827 0.120 14 73186920 missense variant G/C;T snv 6
rs63751165
MAPT
0.925 0.120 17 46010401 missense variant G/A;T snv 3
rs63751223
PSEN1
0.807 0.160 14 73219161 missense variant G/C snv 6
rs63751264
MAPT
0.925 0.120 17 46018726 missense variant A/T snv 2
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63751278
PSEN1
0.827 0.120 14 73173631 missense variant A/G snv 6
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs866604606
MAPK1
0.882 0.120 22 21772907 missense variant G/A snv 4
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