Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2337506
CHRNA7
0.925 0.080 15 32053864 intron variant A/G snv 0.60 2
rs8027814
CHRNA7
0.925 0.080 15 32058469 intron variant G/A snv 0.57 2
rs1884049
ESR1
0.925 0.080 6 151966232 intron variant T/C snv 0.75 2
rs373885474
GRN
0.925 0.080 17 44352061 missense variant C/A;T snv 7.2E-05 2
rs3087258
IL1B
0.925 0.080 2 112837294 upstream gene variant G/A snv 2
rs112451138
PSEN1
0.925 0.080 14 73192667 missense variant T/C snv 7.0E-06 2
rs63750324
PSEN1
0.925 0.080 14 73198111 missense variant C/T snv 2
rs8126696 0.882 0.080 21 37358422 intron variant T/C snv 0.64 3
rs767425642
ACE
0.882 0.120 17 63489010 missense variant G/A;T snv 3.2E-05; 4.0E-06 3
rs748703149
APOE
0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 3
rs529782627
APP
0.882 0.120 21 26112051 missense variant C/A snv 4.0E-06 7.0E-06 3
rs533667466
APP
0.925 0.080 21 25911912 missense variant T/C snv 3
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3
rs901115236
CHCHD10 ; LOC107985577
0.882 0.120 22 23767531 missense variant G/A;T snv 1.5E-05; 1.5E-05 3
rs950530102
DST
0.882 0.160 6 56704357 missense variant C/T snv 3
rs9397456
ESR1
0.882 0.160 6 151926017 intron variant A/G;T snv 3
rs2420616
GRK5
0.882 0.080 10 119316984 intron variant A/G snv 0.69 3
rs4752293
GRK5
0.882 0.080 10 119342186 intron variant C/T snv 0.74 3
rs553119528
GRN
0.882 0.160 17 44352489 missense variant G/A snv 5.2E-05 6.3E-05 3
rs6489630
NTF3
0.882 0.080 12 5495458 intron variant T/C snv 0.75 3
rs2235751
PDYN-AS1 ; PDYN
0.882 0.120 20 1989288 intron variant A/G snv 0.40 3
rs63751399
PSEN1
0.882 0.120 14 73171047 missense variant T/A;C snv 3
rs142690225
PSEN2
0.925 0.080 1 226894111 missense variant G/A snv 1.1E-04 1.1E-04 3
rs4879809
SIGMAR1
0.882 0.120 9 34635601 3 prime UTR variant T/A;C;G snv 1.1E-03; 1.00 3
rs1043202
SMUG1
0.882 0.080 12 54182178 missense variant T/A snv 3