Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs701428
RTN4R
1.000 0.040 22 20241019 downstream gene variant A/G snv 0.56 4
rs7759855 0.925 0.040 6 28315086 downstream gene variant A/G snv 2.8E-02 3
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs2709722
RPL23P8
1.000 0.040 7 20828189 downstream gene variant C/A;T snv 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs6932590 1.000 0.040 6 27281152 downstream gene variant T/C snv 0.26 2
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs2236418
GAD2
0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 4
rs2619538
DTNBP1
0.882 0.040 6 15664978 upstream gene variant A/T snv 0.54 4
rs3761554
GRIA3
1.000 0.040 X 123183391 upstream gene variant T/C snv 0.21 2
rs4281084
NRG1
1.000 0.040 8 31637858 upstream gene variant G/A snv 0.22 2
rs6913660 1.000 0.040 6 27123646 upstream gene variant C/A snv 0.14 2
rs1555910162
SHANK3
0.925 0.080 22 50721469 frameshift variant -/C delins 5
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22