Disease: Alzheimer's Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
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
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs6489630
NTF3
0.882 0.080 12 5495458 intron variant T/C snv 0.75 3
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv 4
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs104894002
LOC105375056 ; TREM2
0.790 0.320 6 41161557 stop gained G/A snv 2.0E-05 2.1E-05 7
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
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1233347077
APOE
0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs17125721
PSEN1
0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121