Disease: Alzheimer's Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1233347077
APOE
0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs748703149
APOE
0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 3
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs223330
CISD2
0.851 0.160 4 102872502 intron variant T/A;C snv 4
rs223331
CISD2
0.851 0.160 4 102872408 intron variant T/A;C snv 5
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv 4
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249