Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs4795541
SLC6A4 ; LOC105371720
0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs267607102
TARDBP
0.851 0.120 1 11022196 missense variant A/G snv 5
rs63750355
CHMP2B
0.827 0.160 3 87253472 stop gained C/T snv 5
rs80356717
TARDBP
0.851 0.120 1 11018836 missense variant A/G snv 5
rs63750092
MAPT
0.882 0.120 17 46014277 missense variant A/T snv 3
rs1163763 0.925 0.120 12 17567834 intron variant G/T snv 0.24 2
rs1319062081
SOD1 ; SCAF4
0.925 0.120 21 31668537 stop gained G/T snv 2
rs536551654
NGFR ; LOC100288866
1.000 0.120 17 49511972 missense variant T/C snv 2
rs1431475678
BDNF ; BDNF-AS
1.000 0.120 11 27658555 missense variant G/C snv 7.0E-06 1
rs706118
BAG1
1.000 0.120 9 33256181 intron variant T/G snv 0.39 1
rs7967622
HNRNPA1
1.000 0.120 12 54284196 intron variant C/T snv 0.76 1
rs741810
FUS
0.925 0.120 16 31182621 synonymous variant C/A;G;T snv 0.32; 4.0E-06; 4.0E-06 2
rs63751243
GRN
0.882 0.160 17 44349190 missense variant C/A;T snv 4.0E-06 4
rs750810467
GRN
1.000 0.120 17 44351420 missense variant G/A;C snv 4.8E-05; 4.0E-06 1
rs63751180
GRN
0.882 0.120 17 44352087 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 3
rs80356726
TARDBP
0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs750444386
NOS1
0.807 0.360 12 117268082 synonymous variant C/A;T snv 4.0E-06; 5.6E-05 6
rs63750129
MAPT
0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs63750349
MAPT
0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
rs17350674
KIF24
1.000 0.120 9 34306412 stop gained C/A;T snv 0.16; 4.1E-06 1
rs1415210991
BDNF
1.000 0.120 11 27701003 5 prime UTR variant G/C snv 4.2E-06 1