Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052352
FUS
0.925 0.120 16 31183958 synonymous variant C/T snv 0.53 0.45 2
rs10814083
KIF24
0.882 0.160 9 34256349 synonymous variant C/T snv 0.40 0.34 3
rs1133763
CCL8
0.882 0.200 17 34320812 missense variant A/C snv 0.21 0.15 4
rs1163763 0.925 0.120 12 17567834 intron variant G/T snv 0.24 2
rs121909335
VCP
0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 9
rs1319062081
SOD1 ; SCAF4
0.925 0.120 21 31668537 stop gained G/T snv 2
rs1390191775
UBQLN2
1.000 0.120 X 56564879 missense variant A/C;G snv 5.5E-06; 5.5E-06 1
rs1415210991
BDNF
1.000 0.120 11 27701003 5 prime UTR variant G/C snv 4.2E-06 1
rs1417841099
ELANE
1.000 0.120 19 852917 missense variant C/G snv 4.6E-06 1
rs1431475678
BDNF ; BDNF-AS
1.000 0.120 11 27658555 missense variant G/C snv 7.0E-06 1
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs17350674
KIF24
1.000 0.120 9 34306412 stop gained C/A;T snv 0.16; 4.1E-06 1
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs2234253
TREM2 ; LOC105375056
0.827 0.120 6 41161367 missense variant G/A;C;T snv 1.9E-04; 1.0E-02 5
rs267607102
TARDBP
0.851 0.120 1 11022196 missense variant A/G snv 5
rs3173615
TMEM106B
0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs4795541
SLC6A4 ; LOC105371720
0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs4859147
DCUN1D1
1.000 0.120 3 182964065 intron variant T/C snv 0.56 0.48 1
rs533451404
GRN
0.925 0.120 17 44349267 missense variant G/A snv 1.6E-05 2.1E-05 2
rs536551654
NGFR ; LOC100288866
1.000 0.120 17 49511972 missense variant T/C snv 2
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17