Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs9357271
BTBD9
0.776 0.160 6 38398097 intron variant T/C snv 0.38 8
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs2251214
SYT1
0.827 0.040 12 79430071 intron variant A/G;T snv 7
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs3743078
CHRNA3
0.807 0.160 15 78602417 intron variant C/A;G snv 7
rs6782011
GRM7
0.807 0.120 3 7457960 intron variant C/T snv 0.52 7
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6