Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs3756007
GABRA2
1.000 0.080 4 46389047 5 prime UTR variant T/C snv 5.4E-02 2
rs3782025
HTR3B
0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs3811939
CRHBP
1.000 0.080 5 76954762 intron variant G/A snv 0.27 2
rs4432372
PIP5K1C
1.000 0.080 19 3698844 intron variant A/G;T snv 1
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs463379
SLC6A3
0.882 0.080 5 1431049 intron variant G/C snv 0.31 3
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4807493
PIP5K1C
1.000 0.080 19 3631038 3 prime UTR variant A/G snv 0.84 1
rs4964057
ARNTL2
0.882 0.080 12 27363909 intron variant T/G snv 0.29 3
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs536599 1.000 0.080 4 46196917 intergenic variant G/T snv 0.47 2
rs56013859
PER2
0.925 0.080 2 238276865 intron variant T/C snv 0.11 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6350
SLC6A3
0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3
rs6473797
OPRK1
0.925 0.080 8 53240422 intron variant T/C snv 0.39 2
rs6923761
GLP1R
0.851 0.200 6 39066296 missense variant G/A;C snv 0.23; 4.0E-06 4
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs6990313
GATA4
1.000 0.080 8 11712527 intron variant G/T snv 0.14 1