Disease: Alzheimer's Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs12425791 0.882 0.120 12 674318 downstream gene variant G/A;C snv 4
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs11542041
APOE
0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 13
rs63750671
APP
0.790 0.240 21 25891858 missense variant G/C snv 8
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs2986017
CALHM1
0.851 0.120 10 103458495 missense variant A/G snv 0.79 0.80 6
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs4986938
ESR2
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35