Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs5905512
MAOB
1.000 0.040 X 43867148 intron variant A/G snv 2
rs6081541
SLC24A3
1.000 0.040 20 19232246 intron variant A/G snv 0.20 2
rs4583255
TAOK2
16 29977620 intron variant A/G snv 0.36 1
rs751229
DISC1 ; TSNAX-DISC1
1.000 0.040 1 231632793 intron variant A/G;T snv 2
rs2958182
TCF4-AS1 ; TCF4
0.882 0.040 18 55481790 intron variant A/T snv 0.72 5
rs165940
LOC107986348 ; PDE4D
0.925 0.040 5 59383658 intron variant A/T snv 0.38 4
rs2619538
DTNBP1
0.882 0.040 6 15664978 upstream gene variant A/T snv 0.54 4
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 3
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs781720548
CPNE1 ; RBM12
0.882 0.040 20 35652946 stop gained C/A snv 5
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
rs3752088
MAPK4
1.000 0.040 18 50714891 intron variant C/A snv 0.51 2
rs6913660 1.000 0.040 6 27123646 upstream gene variant C/A snv 0.14 2
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs2619539
DTNBP1
0.925 0.040 6 15620624 intron variant C/A;G snv 3
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs2498804
LOC102723342 ; SIVA1 ; LOC107987209
0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs778294
DAOA ; DAOA-AS1
0.851 0.040 13 105489886 synonymous variant C/A;T snv 0.27; 4.0E-06 0.26 5
rs2709722
RPL23P8
1.000 0.040 7 20828189 downstream gene variant C/A;T snv 2