Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1386483
TPH2
0.790 0.080 12 72018714 intron variant T/C snv 0.53 9
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs766288
TSNAX-DISC1 ; TSNAX
0.790 0.080 1 231557942 intron variant G/T snv 0.40 7
rs2076137
MLC1
0.807 0.080 22 50077337 intron variant C/T snv 0.14 6
rs2235349
MLC1
0.807 0.080 22 50079810 intron variant T/C snv 0.22 6
rs2812393
TSNAX-DISC1 ; DISC1
0.807 0.080 1 231777927 intron variant G/C snv 0.61 6
rs707284
ERBB4
0.807 0.080 2 211974321 intron variant T/A;C snv 6
rs1106854
TACR1
0.827 0.080 2 75050887 intron variant T/C;G snv 5
rs1386482
TPH2
0.827 0.080 12 72018792 intron variant T/G snv 0.52 5
rs1386486
TPH2
0.827 0.080 12 72018440 intron variant A/G snv 0.53 5
rs166508
ITGA9
0.827 0.080 3 37548944 intron variant T/C snv 0.44 5
rs839523
ERBB4
0.827 0.080 2 211951364 intron variant C/T snv 0.40 5
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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs169068
SSTR5-AS1 ; SSTR5
0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12
rs4988483
SSTR5-AS1 ; SSTR5
0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs1469698992
NUP214
0.776 0.080 9 131190453 missense variant G/A snv 8
rs147837176
SLC6A3
0.776 0.080 5 1400949 missense variant T/C snv 3.1E-04 2.8E-04 8