Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs80356726
TARDBP
0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs63751294
GRN
0.827 0.120 17 44352404 stop gained C/T snv 8.0E-06 6
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
rs80356717
TARDBP
0.851 0.120 1 11018836 missense variant A/G snv 5
rs63750129
MAPT
0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs747019990
PRNP
0.851 0.120 20 4699336 missense variant C/T snv 3.6E-05 7.0E-06 4
rs763841075
GRN
0.851 0.120 17 44350293 missense variant T/C snv 1.8E-04 1.1E-04 4
rs63750092
MAPT
0.882 0.120 17 46014277 missense variant A/T snv 3
rs63751180
GRN
0.882 0.120 17 44352087 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 3
rs1052352
FUS
0.925 0.120 16 31183958 synonymous variant C/T snv 0.53 0.45 2
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
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
rs741810
FUS
0.925 0.120 16 31182621 synonymous variant C/A;G;T snv 0.32; 4.0E-06; 4.0E-06 2
rs752076094
FUS
0.925 0.120 16 31185175 missense variant A/G snv 8.4E-06 2.8E-05 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
rs17350674
KIF24
1.000 0.120 9 34306412 stop gained C/A;T snv 0.16; 4.1E-06 1
rs4859147
DCUN1D1
1.000 0.120 3 182964065 intron variant T/C snv 0.56 0.48 1