Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6489630
NTF3
0.882 0.080 12 5495458 intron variant T/C snv 0.75 3
rs748703149
APOE
0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 3
rs766647311
TREML1 ; LOC105375056 ; TREM2
0.882 0.080 6 41159841 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs8126696 0.882 0.080 21 37358422 intron variant T/C snv 0.64 3
rs112451138
PSEN1
0.925 0.080 14 73192667 missense variant T/C snv 7.0E-06 2
rs1884049
ESR1
0.925 0.080 6 151966232 intron variant T/C snv 0.75 2
rs2337506
CHRNA7
0.925 0.080 15 32053864 intron variant A/G snv 0.60 2
rs3087258
IL1B
0.925 0.080 2 112837294 upstream gene variant G/A snv 2
rs373885474
GRN
0.925 0.080 17 44352061 missense variant C/A;T snv 7.2E-05 2
rs63750324
PSEN1
0.925 0.080 14 73198111 missense variant C/T snv 2
rs8027814
CHRNA7
0.925 0.080 15 32058469 intron variant G/A snv 0.57 2
rs33939927
LRRK2
0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs104893875
SNCA
0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs2298813
SORL1
0.790 0.120 11 121522975 missense variant G/A;T snv 7.2E-02; 4.0E-06 7
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs765670175
PSEN1
0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7