Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1555939456
RPS6KA3
0.851 0.200 X 20187956 missense variant T/C snv 21
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
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
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
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7