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
rs63750129
MAPT
0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs63750306
PSEN1
0.701 0.320 14 73173663 missense variant A/C;G;T snv 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs63750450
PSEN1
0.851 0.120 14 73173571 missense variant A/G snv 4
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
rs63751278
PSEN1
0.827 0.120 14 73173631 missense variant A/G snv 6
rs773403329
SLCO6A1
0.925 0.120 5 102419925 missense variant A/G snv 4.1E-06 7.0E-06 2
rs544706237
REG1A
0.851 0.120 2 79121649 missense variant A/G;T snv 8.0E-06; 5.2E-05 5
rs63751287
PSEN1
0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs1566650594
PSEN1
0.851 0.120 14 73206384 splice acceptor variant A/T snv 4
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
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs3173615
TMEM106B
0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs387906711
UBQLN2
0.807 0.120 X 56565389 missense variant C/A;T snv 6.6E-06 6
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1401496725
REG1A
0.925 0.120 2 79121657 missense variant C/G;T snv 8.0E-06; 8.0E-06 2
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8