Disease: Alzheimer's Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10399931
CHI3L1
0.807 0.320 1 203186952 upstream gene variant T/A;C snv 6
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1138272
GSTP1
0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs1544210 0.882 0.240 10 92728044 regulatory region variant G/A snv 0.39 3
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs163182
KCNQ1
0.882 0.160 11 2822986 intron variant G/A;C snv 3
rs16847897
LRRC31
0.851 0.320 3 169850328 intron variant G/A;C snv 4
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17747324
TCF7L2
0.925 0.160 10 112992744 intron variant T/C snv 0.17 4
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68