Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs17746510
RAPGEF4
0.882 0.080 2 173019562 intron variant T/C;G snv 5
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs727502818
KCNC1
0.790 0.160 11 17772053 missense variant G/A snv 26
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs4818
COMT ; MIR4761
0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 6
rs63750215
PSEN2
0.701 0.240 1 226885603 missense variant A/T snv 19
rs139650807
LRP10
0.925 0.080 14 22875867 missense variant T/A;C snv 6.0E-05 3
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs9951307
AQP4-AS1
0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs3763043
AQP4 ; AQP4-AS1
0.925 0.080 18 26855854 3 prime UTR variant C/T snv 0.30 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
rs73643144
TEK
9 27126454 intron variant T/C snv 3.5E-02 1
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237