Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11989919
NRG1
0.882 0.040 8 32645107 intron variant T/C snv 0.10 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs2979204 0.925 0.040 8 8441347 regulatory region variant T/C snv 0.34 3
rs6771023
GSK3B
0.882 0.040 3 119974764 intron variant T/C snv 0.22 3
rs946903
BCL9
0.882 0.040 1 147625465 3 prime UTR variant T/C snv 0.25 3
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs10884216
LINC02627
0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs1352618632
STARD13
0.925 0.040 13 33112802 missense variant T/C snv 4.0E-06 2
rs17156280
CACNA2D1
0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02 2
rs130058
HTR1B ; LOC105377864
0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs6320
HTR5A-AS1 ; HTR5A
0.925 0.040 7 155070911 synonymous variant T/A;G snv 0.26; 1.2E-05 2
rs208294
P2RX7 ; LOC105370032
0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs6195
NR3C1
0.807 0.120 5 143399752 missense variant T/A;C snv 6
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs2710117
CNTNAP2
0.882 0.040 7 147904680 intron variant T/A snv 0.63 3
rs352759
TUSC3
0.925 0.040 8 15742205 intron variant T/A snv 3