Disease: Alzheimer's Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1233347077
APOE
0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
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
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs2618516
SPON1
0.882 0.080 11 14000092 intron variant T/C snv 0.65 3
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs63750004
PSEN1
0.851 0.080 14 73173655 missense variant T/A;C snv 4
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs63750151
APP
0.882 0.080 21 25891761 missense variant C/G;T snv 3