Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs57095329
MIR3142HG
0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 8
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs10524523
TOMM40
0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 7
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs9951307
AQP4-AS1
0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs63751011
MAPT
0.925 0.120 17 46010418 intron variant C/T snv 4
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 3
rs3763040
AQP4 ; AQP4-AS1
0.925 0.080 18 26864410 intron variant G/A;T snv 3
rs3875089
AQP4 ; AQP4-AS1
0.925 0.080 18 26865469 intron variant T/C snv 0.19 3
rs55781031
BCHE
0.925 0.080 3 165786432 intron variant A/G snv 5.3E-02 3
rs62256378
SUCLG2
0.925 0.080 3 67406609 intron variant G/A;C snv 3
rs6910730
TREM1
0.925 0.080 6 41278895 intron variant A/G snv 0.21 3
rs1157659 1.000 0.040 11 27736075 intron variant A/G snv 0.37 2
rs115881343
TOMM40
1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02 2