Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1173546708
TPH1
0.851 0.120 11 18040661 synonymous variant G/A snv 4.0E-06 5
rs10801152
LOC105371665
1.000 0.040 1 192792174 intron variant A/T snv 0.31 1
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs1819741 1.000 0.040 1 192815708 intron variant T/A;C snv 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs860554
PKP1
1.000 0.040 1 201293304 intron variant C/G;T snv 1
rs4977831
FOCAD
1.000 0.040 9 20713069 intron variant A/G;T snv 1
rs2039391
FOCAD
1.000 0.040 9 20714015 intron variant C/T snv 0.86 1
rs11805657
RGS7
1.000 0.040 1 240955726 intron variant T/C snv 0.87 1
rs5751876
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs1800857
CCKAR
0.851 0.120 4 26489489 splice region variant A/G snv 0.17 0.18 4
rs1800855
CCKAR
0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 2
rs17466684
EPHX2
0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs7103411
BDNF ; BDNF-AS
0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs140701
SLC6A4
0.790 0.200 17 30211514 intron variant C/T snv 0.40 7
rs4583306
SLC6A4
1.000 0.040 17 30211697 intron variant A/G snv 0.37 1
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs2271933
HCRTR1
0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs2910931
MIR579 ; ZFR
0.925 0.080 5 32394809 intron variant T/A snv 0.63 3