Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs1015443
PRH1-PRR4 ; PRR4 ; TAS2R13 ; PRH1
0.925 0.160 12 10908523 missense variant T/A;C snv 4.0E-06; 0.59 2
rs2836016
KCNJ6
0.925 0.080 21 37840718 intron variant G/A snv 0.59 0.58 2
rs2074957
PIP5K1C
1.000 0.080 19 3653527 synonymous variant C/A;T snv 8.0E-06; 0.57 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs1799913
TPH1
0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs6923761
GLP1R
0.851 0.200 6 39066296 missense variant G/A;C snv 0.23; 4.0E-06 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs6350
SLC6A3
0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs7958822
ARNTL2
0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5