Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12604324
OSBPL1A
1.000 0.080 18 24164468 intron variant G/A snv 0.18 1
rs1741309
SMOX
1.000 0.080 20 4163930 intron variant A/G snv 0.53 1
rs41526548 1.000 0.080 9 92129496 upstream gene variant T/C snv 1
rs571825723
PSEN1
0.925 0.080 14 73211867 missense variant C/T snv 4.4E-05 2.8E-05 4
rs63751011
MAPT
0.925 0.120 17 46010418 intron variant C/T snv 4
rs1341026713
APP
0.925 0.080 21 25955719 missense variant G/A snv 4.0E-06 1.4E-05 3
rs142690225
PSEN2
0.925 0.080 1 226894111 missense variant G/A snv 1.1E-04 1.1E-04 3
rs533667466
APP
0.925 0.080 21 25911912 missense variant T/C snv 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
rs3824968
SORL1
0.925 0.080 11 121605213 synonymous variant T/A snv 0.39 0.29 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
rs1401663578
ACE
0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 4
rs763872192
CD36
0.882 0.080 7 80672000 missense variant C/T snv 2.8E-05 4
rs1010159
SORL1
0.882 0.080 11 121612692 non coding transcript exon variant C/T snv 0.55 0.55 3
rs1043202
SMUG1
0.882 0.080 12 54182178 missense variant T/A snv 3
rs2235751
PDYN-AS1 ; PDYN
0.882 0.120 20 1989288 intron variant A/G snv 0.40 3
rs2420616
GRK5
0.882 0.080 10 119316984 intron variant A/G snv 0.69 3
rs2618516
SPON1
0.882 0.080 11 14000092 intron variant T/C snv 0.65 3
rs4752293
GRK5
0.882 0.080 10 119342186 intron variant C/T snv 0.74 3
rs4879809
SIGMAR1
0.882 0.120 9 34635601 3 prime UTR variant T/A;C;G snv 1.1E-03; 1.00 3