Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs1131445
IL16 ; STARD5
0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs3219151
GABRA6
0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs578776
CHRNA3
0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 13
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs165774
COMT
0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27 11
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs11568817
HTR1B ; LOC105377864
0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs130058
HTR1B ; LOC105377864
0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8