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
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63750900
PSEN1
0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 9
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
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
rs387906711
UBQLN2
0.807 0.120 X 56565389 missense variant C/A;T snv 6.6E-06 6
rs63750512
MAPT
0.827 0.160 17 46024010 missense variant G/A;C snv 1.2E-05 6
rs63750869
MAPT
0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 6
rs63751068
PSEN1
0.827 0.120 14 73186920 missense variant G/C;T snv 6
rs63751223
PSEN1
0.807 0.160 14 73219161 missense variant G/C snv 6
rs63751278
PSEN1
0.827 0.120 14 73173631 missense variant A/G snv 6
rs63751294
GRN
0.827 0.120 17 44352404 stop gained C/T snv 8.0E-06 6
rs661
PSEN1
0.807 0.120 14 73217225 missense variant G/A;T snv 4.0E-06 6
rs80356715
TARDBP
0.807 0.120 1 11016874 missense variant C/G;T snv 8.0E-06; 2.2E-04 6
rs121909331
VCP
0.851 0.200 9 35064167 missense variant G/T snv 5
rs1314736087
SYBU
0.851 0.120 8 109575782 frameshift variant GA/- delins 4.0E-06 5
rs544706237
REG1A
0.851 0.120 2 79121649 missense variant A/G;T snv 8.0E-06; 5.2E-05 5
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
rs63750349
MAPT
0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
rs63750635
MAPT
0.851 0.120 17 46014286 missense variant C/T snv 5