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
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
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
rs2298813
SORL1
0.790 0.120 11 121522975 missense variant G/A;T snv 7.2E-02; 4.0E-06 7
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs28936380
PSEN2
0.827 0.080 1 226885546 missense variant C/G;T snv 1.2E-05 5
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs6332
NTF3
0.851 0.080 12 5494466 synonymous variant G/A;T snv 0.49; 3.2E-05 4
rs63749824
PSEN1
0.776 0.120 14 73170945 missense variant C/G;T snv 4.0E-06; 1.2E-05 8
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
rs63750082
PSEN1
0.732 0.120 14 73192712 missense variant G/C;T snv 8.0E-06 13
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
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17