Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 9
rs6438552
GSK3B
0.790 0.280 3 119912967 intron variant A/G snv 0.54 9
rs1322643228
TXNRD1
0.807 0.280 12 104321110 missense variant C/T snv 7.1E-06 6
rs3755557
GSK3B ; LOC107986119
0.807 0.280 3 120096110 non coding transcript exon variant T/A snv 0.14 6
rs5326
DRD1
0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6
rs1182593032
NQO1
0.851 0.200 16 69718516 missense variant A/G snv 4
rs1231813088
HHEX
0.851 0.160 10 92690015 missense variant C/T snv 4
rs1322425552
OTOP2 ; USH1G
0.851 0.160 17 74923048 missense variant G/A snv 4
rs1457049406
MIR4761 ; COMT
0.851 0.200 22 19962555 missense variant C/T snv 4
rs4790953 0.851 0.160 17 65230912 downstream gene variant A/C snv 0.17 4
rs6805251
GSK3B
0.925 0.120 3 119841759 intron variant T/A;C snv 4
rs1330075052
TXNRD1
0.882 0.160 12 104215828 missense variant T/C snv 1.4E-05 3
rs1338719
PDE4B
0.925 0.120 1 66183851 intron variant C/T snv 0.49 2
rs1447119000
LOC112268294 ; CYP2D6 ; NDUFA6-DT
0.925 0.120 22 42130763 missense variant G/A snv 2
rs1890196
PDE4B
0.925 0.120 1 66337397 intron variant C/G;T snv 2
rs2015586
SLC18A2
0.925 0.120 10 117262226 intron variant C/T snv 0.58 2
rs2445142
HSPG2
0.925 0.120 1 21899250 intron variant G/A;C snv 2
rs2603751
NR4A1
0.925 0.120 12 52059498 3 prime UTR variant T/C snv 0.25 2
rs265975 0.925 0.120 5 175435192 downstream gene variant C/T snv 0.43 2