Disease: Alzheimer's Disease
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 58
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs1362575880
PSEN1
0.851 0.120 14 73192840 missense variant A/C snv 4.0E-06 4
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs1424266770
CASP3
0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 201
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 230
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 68
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs35870237
LRRK2
0.763 0.120 12 40340404 missense variant T/C snv 8
rs371425292
APP
0.763 0.160 21 25897627 missense variant C/A;T snv 8.0E-06 10
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11