Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1143684
NQO2
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84 4
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 6
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 3
rs4646
MIR4713HG ; CYP19A1
0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs9951307
AQP4-AS1
0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs469083
MX1
1.000 0.040 21 41436789 intron variant C/T snv 0.61 2
rs7700443 5 85876294 intergenic variant T/G snv 0.57 1
rs363050
SNAP25-AS1 ; SNAP25
0.790 0.240 20 10253609 intron variant G/A snv 0.57 8
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs17518584
CADM2
0.827 0.160 3 85555773 intron variant C/T snv 0.50 8
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs1557372 1.000 0.040 21 41460614 downstream gene variant C/T snv 0.40 2
rs1157659 1.000 0.040 11 27736075 intron variant A/G snv 0.37 2
rs2162560
DNMT1
1.000 0.040 19 10168778 intron variant G/A snv 0.35 2
rs457274
MX1
1.000 0.040 21 41420558 5 prime UTR variant C/G snv 0.35 2
rs3763043
AQP4 ; AQP4-AS1
0.925 0.080 18 26855854 3 prime UTR variant C/T snv 0.30 3
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 8
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs10073892
SLCO6A1
5 102391066 non coding transcript exon variant T/C snv 0.24 0.21 1
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135