Disease: Alzheimer's Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs63750301
PSEN1
0.827 0.120 14 73198052 missense variant C/T snv 4.0E-06 6
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63750004
PSEN1
0.851 0.080 14 73173655 missense variant T/A;C snv 4
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs6332
NTF3
0.851 0.080 12 5494466 synonymous variant G/A;T snv 0.49; 3.2E-05 4
rs6330
NGF ; NGF-AS1
0.763 0.240 1 115286692 missense variant G/A snv 0.37 0.36 12
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs5930
MIR6886 ; LDLR
0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 8
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30