Disease: Attention deficit hyperactivity disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
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
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
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
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs5751876
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs7194256
SLC6A2
0.827 0.120 16 55703779 3 prime UTR variant C/G;T snv 7
rs1843809
TPH2
0.851 0.080 12 71954918 intron variant G/T snv 0.77 6