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
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1182182524
MAPT
0.882 0.120 17 45983724 missense variant T/G snv 1.4E-05 3
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
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs121909331
VCP
0.851 0.200 9 35064167 missense variant G/T snv 5
rs1235948930
MAPT
0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 4
rs1295855402
MAPT
0.925 0.120 17 46024034 missense variant C/T snv 7.0E-06 2
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs1566650594
PSEN1
0.851 0.120 14 73206384 splice acceptor variant A/T snv 4
rs1595014 0.882 0.120 7 12148903 intergenic variant T/A snv 0.23 3
rs1804469
MSMB ; LOC105378287
0.925 0.120 10 46033495 missense variant T/C snv 2
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs63749836
PSEN1
0.827 0.160 14 73192786 missense variant G/A snv 5
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs63750053
PSEN1
0.827 0.120 14 73192721 missense variant G/T snv 5
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs63750450
PSEN1
0.851 0.120 14 73173571 missense variant A/G snv 4