Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs63750083
PSEN1
0.732 0.160 14 73219177 missense variant C/A;T snv 13
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs4717806
LOC105375350 ; STX1A ; BUD23
0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs754203
CYP46A1
0.807 0.200 14 99691630 non coding transcript exon variant A/G snv 0.27 6
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 5
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5
rs8702
KLC1
0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs11637611
PARP6
0.851 0.160 15 72259371 intron variant C/T snv 0.63 4
rs11767557
EPHA1-AS1
0.882 0.080 7 143412046 intron variant T/C snv 0.18 4
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
rs12752888
LINC02784
0.851 0.160 1 54527266 downstream gene variant T/C snv 0.26 4
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs391300
SRR
0.882 0.160 17 2312964 intron variant T/C snv 0.58 4
rs541458 0.851 0.080 11 86077309 regulatory region variant C/T snv 0.71 4
rs59007384
TOMM40
0.851 0.080 19 44893408 intron variant G/A;T snv 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs7840202
UBR5
0.851 0.160 8 102296172 intron variant A/C snv 0.21 4