Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs2498804
LOC102723342 ; SIVA1 ; LOC107987209
0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 6
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs1867283
NTRK2
0.925 0.080 9 84835851 intron variant G/A snv 0.39 5
rs2958182
TCF4-AS1 ; TCF4
0.882 0.040 18 55481790 intron variant A/T snv 0.72 5
rs6465084
LOC105375382 ; GRM3
0.851 0.040 7 86774159 intron variant A/G snv 0.26 5
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4