Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800866
SIGMAR1
0.851 0.080 9 34637693 missense variant T/G snv 0.20 0.18 8
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs63751037
PSEN1
0.790 0.080 14 73173642 missense variant A/G snv 6
rs669
A2M ; KLRG1
0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 6
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs2306604
TFAM
0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs9468
MAPT
0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 5
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs12344615
UBQLN1
0.851 0.080 9 83666280 intron variant A/C;G snv 4
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs2070045
SORL1
0.851 0.080 11 121577381 synonymous variant T/G snv 0.32 0.23 4
rs28936380
PSEN2
0.827 0.080 1 226885546 missense variant C/G;T snv 1.2E-05 4
rs3755166
LRP2
1.000 0.080 2 169363371 upstream gene variant A/C;G snv 4
rs541458 0.851 0.080 11 86077309 regulatory region variant C/T snv 0.71 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 4
rs6332
NTF3
0.851 0.080 12 5494466 synonymous variant G/A;T snv 0.49; 3.2E-05 4
rs63750050
PSEN1
0.925 0.080 14 73198106 missense variant T/G snv 4
rs63750444
PSEN1
0.882 0.080 14 73192745 missense variant G/A snv 4
rs63751106
PSEN1
0.827 0.080 14 73173643 missense variant T/A;C snv 4
rs9331896
CLU ; MIR6843
0.851 0.080 8 27610169 intron variant C/G;T snv 4
rs9357347
LOC107986595
0.851 0.080 6 41182853 intergenic variant A/C;T snv 4
rs1010159
SORL1
0.882 0.080 11 121612692 non coding transcript exon variant C/T snv 0.55 0.55 3
rs11724635
BST1
0.925 0.080 4 15735478 intron variant C/A;G snv 0.43 3