Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs265975 0.925 0.120 5 175435192 downstream gene variant C/T snv 0.43 2
rs7669317 0.925 0.120 4 105536173 downstream gene variant T/C snv 2.9E-02 2
rs767413934
DRD2
0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06 2
rs4739217
GFRA2
0.925 0.120 8 21727549 intron variant G/C snv 0.39 2
rs6587002
GFRA2
0.925 0.120 8 21723708 intron variant T/C;G snv 2
rs6988470
GFRA2
0.925 0.120 8 21742957 intron variant T/C snv 0.58 2
rs3943552
GLI2
0.925 0.120 2 120824482 intron variant C/T snv 0.14 2
rs9878473
GSK3B
0.925 0.120 3 119931941 intron variant T/C snv 0.54 2
rs2445142
HSPG2
0.925 0.120 1 21899250 intron variant G/A;C snv 2
rs878949
HSPG2
0.925 0.120 1 21900598 intron variant T/C snv 0.52 2
rs7620754
LOC107986115
0.925 0.120 3 114229128 intron variant T/C snv 0.24 2
rs905568
LOC107986115
0.925 0.120 3 114232449 non coding transcript exon variant C/A;G;T snv 2
rs1447119000
LOC112268294 ; CYP2D6 ; NDUFA6-DT
0.925 0.120 22 42130763 missense variant G/A snv 2
rs2603751
NR4A1
0.925 0.120 12 52059498 3 prime UTR variant T/C snv 0.25 2
rs2701124
NR4A1
0.925 0.120 12 52054373 synonymous variant G/A;C snv 9.5E-02 2
rs1338719
PDE4B
0.925 0.120 1 66183851 intron variant C/T snv 0.49 2
rs1890196
PDE4B
0.925 0.120 1 66337397 intron variant C/G;T snv 2
rs7528545
PDE4B
0.925 0.120 1 66227081 intron variant T/C snv 0.62 2
rs783036
PDE4B
0.925 0.120 1 66365687 synonymous variant G/A snv 0.48 0.56 2
rs37364
PRLR
0.925 0.120 5 35072278 intron variant T/G snv 0.34 2
rs2015586
SLC18A2
0.925 0.120 10 117262226 intron variant C/T snv 0.58 2
rs363224
SLC18A2
0.925 0.120 10 117263062 intron variant C/A snv 0.48 2
rs1045280
ARRB2
0.882 0.160 17 4719343 synonymous variant C/T snv 0.71 0.62 3
rs1402139464
BDNF
0.882 0.160 11 27701009 5 prime UTR variant G/A;T snv 8.4E-06 3
rs201934979
CYP1A2
0.882 0.160 15 74749838 missense variant C/T snv 8.8E-05; 8.0E-06 1.3E-04 3