Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2770292
HTR2A
1.000 0.040 13 46860971 intron variant C/G snv 0.18 1
rs2910931
MIR579 ; ZFR
0.925 0.080 5 32394809 intron variant T/A snv 0.63 3
rs3213207
DTNBP1
0.776 0.120 6 15627871 intron variant T/C snv 8.7E-02 11
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs324891
LINC00461
1.000 0.040 5 88616114 intron variant C/T snv 4.2E-04 1
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs3742278
HTR2A
1.000 0.040 13 46845442 intron variant A/G snv 0.19 1
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs37790 1.000 0.040 5 53346682 intergenic variant C/G;T snv 1
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs3816995
SDK2
1.000 0.040 17 73339121 intron variant G/A snv 0.40 1
rs4076452
LINC02210-CRHR1
1.000 0.040 17 45778528 intron variant G/C snv 0.16 2
rs4145262 1.000 0.040 12 105659532 regulatory region variant C/A snv 4.8E-02 1
rs4448731 1.000 0.040 12 71935326 upstream gene variant T/C snv 0.40 1
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4583306
SLC6A4
1.000 0.040 17 30211697 intron variant A/G snv 0.37 1
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs4760820
TPH2
0.925 0.040 12 72003216 intron variant C/G snv 0.29 2
rs4795942
TMEM132E
1.000 0.040 17 34584149 intron variant C/T snv 0.72 1