Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs80356726
TARDBP
0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs267607102
TARDBP
0.851 0.120 1 11022196 missense variant A/G snv 5
rs80356717
TARDBP
0.851 0.120 1 11018836 missense variant A/G snv 5
rs63750355
CHMP2B
0.827 0.160 3 87253472 stop gained C/T snv 5
rs4859147
DCUN1D1
1.000 0.120 3 182964065 intron variant T/C snv 0.56 0.48 1
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs2234253
TREM2 ; LOC105375056
0.827 0.120 6 41161367 missense variant G/A;C;T snv 1.9E-04; 1.0E-02 5
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs3173615
TMEM106B
0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs121909335
VCP
0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 9
rs10814083
KIF24
0.882 0.160 9 34256349 synonymous variant C/T snv 0.40 0.34 3
rs17350674
KIF24
1.000 0.120 9 34306412 stop gained C/A;T snv 0.16; 4.1E-06 1
rs706118
BAG1
1.000 0.120 9 33256181 intron variant T/G snv 0.39 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1415210991
BDNF
1.000 0.120 11 27701003 5 prime UTR variant G/C snv 4.2E-06 1
rs1431475678
BDNF ; BDNF-AS
1.000 0.120 11 27658555 missense variant G/C snv 7.0E-06 1
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs76980269
NOS1
0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs750444386
NOS1
0.807 0.360 12 117268082 synonymous variant C/A;T snv 4.0E-06; 5.6E-05 6
rs1163763 0.925 0.120 12 17567834 intron variant G/T snv 0.24 2
rs7967622
HNRNPA1
1.000 0.120 12 54284196 intron variant C/T snv 0.76 1