Disease: Alzheimer's Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs104894002
LOC105375056 ; TREM2
0.790 0.320 6 41161557 stop gained G/A snv 2.0E-05 2.1E-05 7
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs28936380
PSEN2
0.827 0.080 1 226885546 missense variant C/G;T snv 1.2E-05 5
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
rs765670175
PSEN1
0.790 0.120 14 73173646 missense variant T/A snv 8.0E-06 7
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
rs748703149
APOE
0.882 0.080 19 44908729 missense variant G/A;C;T snv 6.3E-06; 6.3E-06 3
rs63750301
PSEN1
0.827 0.120 14 73198052 missense variant C/T snv 4.0E-06 6
rs63750900
PSEN1
0.763 0.160 14 73198067 missense variant G/A snv 4.0E-06 7.0E-06 9
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs766647311
TREML1 ; LOC105375056 ; TREM2
0.882 0.080 6 41159841 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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