Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28363170
SLC6A3
0.827 0.120 5 1393745 3 prime UTR variant -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC delins 8.1E-06 7
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs10170218 1.000 0.040 2 187949717 intron variant A/C snv 0.25 1
rs159572
ANKRD55
1.000 0.040 5 56211219 intron variant A/C snv 0.37 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs2271933
HCRTR1
0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs12364283
DRD2 ; LOC105369501
0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs6470292
LOC105375743 ; LINC00964
1.000 0.040 8 124855801 intron variant A/G snv 0.17 2
rs2400207
LOC107986458 ; SH3RF2
1.000 0.040 5 146000534 intron variant A/G snv 0.56 1
rs3852144
C5orf67
1.000 0.040 5 56566769 intron variant A/G snv 0.37 1
rs4511180
PTPRVP
1.000 0.040 1 202180311 non coding transcript exon variant A/G snv 0.65 1
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs2400707
ADRB2
1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 3
rs182455
STMN1 ; LOC105376885
0.925 0.120 1 25908492 upstream gene variant A/G;T snv 2
rs683250
LOC107984425 ; DLG2
1.000 0.040 11 83565125 intron variant A/G;T snv 2
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs10055255
CRHBP
1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48