Variant Name |
Variant Type |
Location in Gene |
Related Gene |
No. of Studies (significant/non-significant/trend) |
DRD4 exon3 VNTR |
VNTR |
exon 3 |
DRD4 |
58 (33/25/0) |
SLC6A3 3'-UTR VNTR |
VNTR |
3' UTR |
SLC6A3 |
55 (22/33/0) |
5HTTLPR |
insertion/deletion |
promoter |
SLC6A4 |
21 (7/14/0) |
DRD5 5'-flanking (CT/GT/GA)n |
microsatellite |
5' flanking, 18.5 kb from the 5' end of the gene DRD5 |
DRD5 |
18 (13/5/0) |
SLC6A4 intron2 VNTR |
VNTR |
intron 2 |
SLC6A4 |
14 (4/10/0) |
DRD4 promoter duplication 120bp |
insertion/deletion |
promoter |
DRD4 |
13 (4/9/0) |
MAOA promoter VNTR |
VNTR |
promoter, 1.2kb upstream of the coding region |
MAOA |
11 (3/8/0) |
SLC6A3 intron8 VNTR |
VNTR |
intron 8 |
SLC6A3 |
11 (5/6/0) |
DBH intron5 C/T TaqI |
point mutation |
intron 5 |
DBH |
8 (4/4/0) |
DRD4 promoter -521C/T |
point mutation |
promoter |
DRD4 |
6 (0/6/0) |
DBH 5'-flanking (GT)n |
microsatellite |
5' flanking, approximately 4.7 kb 5' to the transcriptional start site |
DBH |
5 (0/5/0) |
DRD2 TaqI |
point mutation |
|
DRD2 |
5 (1/4/0) |
DRD4 promoter -616C/G |
point mutation |
promoter |
DRD4 |
5 (1/4/0) |
TH intron1 (TCAT)n |
microsatellite |
intron 1 |
TH |
5 (0/5/0) |
HTR2A T102C |
point mutation |
|
HTR2A |
4 (1/3/0) |
SNAP25 5'-UTR (ATTT)n |
microsatellite |
5' UTR; between the 5' UTR and the first transcribed exon of the SNAP25 gene |
SNAP25 |
4 (2/2/0) |
ADRA2C upstream (TG)n |
microsatellite |
upstream |
ADRA2C |
3 (1/2/0) |
BDNF C270T |
point mutation |
5' UTR |
BDNF |
3 (2/1/0) |
DRD3 exon1 Ser/Gly |
point mutation |
exon 1 |
DRD3 |
3 (0/3/0) |
DRD4 intron1 (G)n |
microsatellite |
intron 1 |
DRD4 |
3 (0/3/0) |
HTR1B G861C |
point mutation |
|
HTR1B |
3 (2/1/0) |
HTR2A His452Tyr |
point mutation |
|
HTR2A |
3 (3/0/0) |
HTR2A promoter 1438G/A |
point mutation |
promoter |
HTR2A |
3 (0/3/0) |
MAOA exon8 941G/T |
point mutation |
exon 8 |
MAOA |
3 (2/1/0) |
MAOA intron2 CA(n) |
microsatellite |
intron 2 |
MAOA |
3 (1/2/0) |
SLC6A2 promoter -3081A/T |
point mutation |
promoter |
SLC6A2 |
3 (2/1/0) |
DBH exon2 444G/A EcoNI |
point mutation |
exon 2 |
DBH |
2 (0/2/0) |
DDC exon1 ins/del 4bp |
insertion/deletion |
exon 1 |
DDC |
2 (0/2/0) |
DRD4 exon1 ins/del 12bp |
insertion/deletion |
exon 1 |
DRD4 |
2 (0/2/0) |
DRD4 promoter -376C/T |
point mutation |
promoter |
DRD4 |
2 (0/2/0) |
DRD5 upstream (TC)n |
microsatellite |
5' flanking and promoter region, 119-182 bp upstream of the transcriptional start site |
DRD5 |
2 (0/2/0) |
HLA-DRB1 alleles01-10 |
HLA-DRB1 alleles |
|
HLA-DRB1 |
2 (1/1/0) |
IL1RN intron2 VNTR |
VNTR |
intron 2 |
IL1RN |
2 (1/1/0) |
MAOA DXS7 |
microsatellite |
Xp11.23-Xp11.4, linked to the MAO gene |
MAOA |
2 (1/1/0) |
SLC6A2 intron9 G/C MnlI |
point mutation |
intron 9 |
SLC6A2 |
2 (0/2/0) |
SLC6A3 3'-flanking D5S2005 |
microsatellite |
3' flanking |
SLC6A3 |
2 (0/2/0) |
SLC6A3 exon9 1342A>G |
point mutation |
exon 9 |
SLC6A3 |
2 (0/2/0) |
SLC6A4 3'-UTR G/T |
point mutation |
3' UTR |
SLC6A4 |
2 (1/1/0) |
TPH1 intron7 A218C |
point mutation |
intron 7 |
TPH1 |
2 (0/2/0) |
AANAT A163V |
point mutation |
|
AANAT |
1 (0/0/1) |
AANAT G177D |
point mutation |
|
AANAT |
1 (0/0/1) |
AANAT V62I |
point mutation |
|
AANAT |
1 (0/0/1) |
ADRA1A Cys492Arg |
point mutation |
|
ADRA1A |
1 (0/1/0) |
ADRA2C C444T |
point mutation |
|
ADRA2C |
1 (0/0/1) |
ASMT D210G |
point mutation |
|
ASMT |
1 (0/0/1) |
ASMT IVS5+2T>C |
point mutation |
|
ASMT |
1 (1/0/0) |
ASMT L298F |
point mutation |
|
ASMT |
1 (0/0/1) |
CALY 3'-flanking Calc4510 C/T |
point mutation |
3' flanking |
CALY |
1 (0/1/0) |
CALY intron2 hCV25595220 C/T |
point mutation |
intron 2 |
CALY |
1 (0/1/0) |
CALY intron5 Calc4760 C/T |
point mutation |
intron 5 |
CALY |
1 (0/1/0) |
CALY intron5 Calc4801 C/A |
point mutation |
intron 5 |
CALY |
1 (0/1/0) |
CALY promoter Calc-189 C/A |
point mutation |
promoter |
CALY |
1 (0/1/0) |
CHRNA4 exon2 150C/T |
point mutation |
exon 2 |
CHRNA4 |
1 (1/0/0) |
CHRNA4 exon2 211A/G |
point mutation |
exon 2 |
CHRNA4 |
1 (1/0/0) |
CHRNA4 exon2 215A/G |
point mutation |
exon 2 |
CHRNA4 |
1 (1/0/0) |
CHRNA4 exon5 T/C CfoI |
point mutation |
exon 5 |
CHRNA4 |
1 (0/1/0) |
CHRNA7 upstream D15S1043 |
microsatellite |
lies 0.5 cM centromeric to D15S165, and maps proximally to the duplicated region. |
CHRNA7 |
1 (0/1/0) |
CHRNA7 upstream D15S1360 |
microsatellite |
lies less than 120 kb upstream from the first exon of CHRNA7 |
CHRNA7 |
1 (0/1/0) |
CHRNA7 upstream D15S165 |
microsatellite |
lies approximately 2 cM centromeric to D15S1360, and between the full length and duplicated genes. |
CHRNA7 |
1 (0/1/0) |
COMT 158G/A |
point mutation |
at codon 158 |
COMT |
1 (0/1/0) |
DBH 5'-flanking ins/del |
insertion/deletion |
5' flanking, approximately 4.7 kb 5' to the transcriptional start site (~6 kb from the intron 5 polymorphism DBH Taq1) |
DBH |
1 (0/1/0) |
DBH intron9 MspI |
point mutation |
intron 9 |
DBH |
1 (0/1/0) |
DDC 3'-flanking D7S2422 |
microsatellite |
3' flanking |
DDC |
1 (1/0/0) |
DDC 5'-flanking D7S2561 |
microsatellite |
5' flanking |
DDC |
1 (0/1/0) |
DRD1 3'-UTR +1403T/C Bsp1286I |
point mutation |
3'-UTR |
DRD1 |
1 (0/1/0) |
DRD1 5'-UTR -48G/A DdeI |
point mutation |
5'-UTR |
DRD1 |
1 (0/1/0) |
DRD1 5'-UTR -800T/C HaeIII |
point mutation |
5'-UTR |
DRD1 |
1 (0/1/0) |
DRD1 upstream -1251G/C HaeIII |
point mutation |
~0.2 kb upstream of one of two promoters for DRD1 |
DRD1 |
1 (0/1/0) |
DRD2 exon7 Ser311Cys |
point mutation |
exon 7 |
DRD2 |
1 (0/1/0) |
DRD2 promoter -241A>G |
point mutation |
promoter |
DRD2 |
1 (0/1/0) |
DRD3 intron5 MspI |
point mutation |
intron 5 |
DRD3 |
1 (0/1/0) |
DRD4 promoter -615A/G |
point mutation |
promoter |
DRD4 |
1 (0/1/0) |
DRD5 3'-flanking D4S615 |
microsatellite |
~131 kb 3' of the DRD5 gene |
DRD5 |
1 (1/0/0) |
DRD5 3'-UTR 1481T/C |
point mutation |
3' UTR |
DRD5 |
1 (1/0/0) |
DRD5 5'-flanking D4S1582 |
microsatellite |
5' flanking, 2 cM from the 5' end of the gene DRD5 |
DRD5 |
1 (1/0/0) |
DRD5 5'-flanking D4S2928 |
microsatellite |
5' flanking, 5.3 cM from the 5' end of the gene DRD5 |
DRD5 |
1 (0/1/0) |
DRD5 T978C |
point mutation |
|
DRD5 |
1 (0/0/1) |
DYX1C1 1249G/T |
point mutation |
coding region |
DYX1C1 |
1 (0/1/0) |
GNAO1 -1214G>A |
point mutation |
|
GNAO1 |
1 (0/1/0) |
GNAO1 IVS4+22T>C |
point mutation |
|
GNAO1 |
1 (0/1/0) |
GNAO1 T(T)513C(T) |
point mutation |
|
GNAO1 |
1 (0/1/0) |
GNAT2 1259 1282del |
insertion/deletion |
|
GNAT2 |
1 (0/1/0) |
GNAT2 -32A>G |
point mutation |
|
GNAT2 |
1 (1/0/0) |
GNAT2 C(L)319A(I) |
point mutation |
|
GNAT2 |
1 (0/1/0) |
GNAT2 G(T)546A(T) |
point mutation |
|
GNAT2 |
1 (0/1/0) |
GNAT2 G(V)370A(M) |
point mutation |
|
GNAT2 |
1 (0/1/0) |
GNAT2 T(N)933C(N) |
point mutation |
|
GNAT2 |
1 (0/1/0) |
GNAZ 1368G>C |
point mutation |
|
GNAZ |
1 (0/1/0) |
GNAZ 1479A>G |
point mutation |
|
GNAZ |
1 (0/1/0) |
GNAZ 2418A>G |
point mutation |
|
GNAZ |
1 (0/1/0) |
GNAZ 2529T>C |
point mutation |
|
GNAZ |
1 (0/1/0) |
GPR50 Del502-505 |
insertion/deletion |
|
GPR50 |
1 (0/0/1) |
GPR50 I606V |
point mutation |
|
GPR50 |
1 (0/0/1) |
GPR50 S493R |
point mutation |
|
GPR50 |
1 (0/0/1) |
GPR50 T532A |
point mutation |
|
GPR50 |
1 (0/0/1) |
GRIN2A 3'-UTR #5765C/T |
point mutation |
3' UTR |
GRIN2A |
1 (0/1/0) |
GRIN2A exon10 G695A |
point mutation |
exon 10 |
GRIN2A |
1 (0/1/0) |
GRIN2A exon5 G325A |
point mutation |
exon 5 |
GRIN2A |
1 (1/0/0) |
GRIN2A exon6 G/A |
point mutation |
exon 6 |
GRIN2A |
1 (0/1/0) |
GSK3B -50C/T |
point mutation |
|
GSK3B |
1 (0/1/0) |
GSK3B -1727A/T |
point mutation |
|
GSK3B |
1 (1/0/0) |
HTR1A C-1019G |
point mutation |
|
HTR1A |
1 (1/0/0) |
HTR1B A-161T |
point mutation |
|
HTR1B |
1 (0/1/0) |
HTR1D 1350T>C |
point mutation |
coding region |
HTR1D |
1 (0/1/0) |
HTR1D 3'-UTR 1236A>G |
point mutation |
3' UTR |
HTR1D |
1 (1/0/0) |
HTR4 -36C>T |
point mutation |
|
HTR4 |
1 (0/1/0) |
HTR4 83097C>T |
point mutation |
|
HTR4 |
1 (0/1/0) |
HTR4 83198A>G |
point mutation |
|
HTR4 |
1 (0/1/0) |
HTR5A 12A>T |
point mutation |
|
HTR5A |
1 (0/1/0) |
HTR5A -19G>C |
point mutation |
|
HTR5A |
1 (0/1/0) |
HTR6 267C>T |
point mutation |
|
HTR6 |
1 (0/1/0) |
LPHN3 1394G>A |
point mutation |
|
LPHN3 |
1 (0/0/1) |
LPHN3 1670G>A |
point mutation |
|
LPHN3 |
1 (0/0/1) |
LPHN3 1869-13T>C |
point mutation |
intron |
LPHN3 |
1 (0/0/1) |
LPHN3 2348C>T |
point mutation |
|
LPHN3 |
1 (0/0/1) |
LPHN3 3387+36A>G |
point mutation |
intron |
LPHN3 |
1 (0/0/1) |
LPHN3 471G>A |
point mutation |
|
LPHN3 |
1 (0/0/1) |
LPHN3 839G>T |
point mutation |
|
LPHN3 |
1 (0/0/1) |
MAOB (GT)n |
microsatellite |
|
MAOB |
1 (0/1/0) |
MAOB exon15 2276T>C |
point mutation |
exon 15 |
MAOB |
1 (1/0/0) |
MAOB exon15 2327T>C |
point mutation |
exon 15 |
MAOB |
1 (1/0/0) |
MOG exon3 Val145Ile |
point mutation |
exon 3 |
MOG |
1 (0/1/0) |
MOG upstream (CA)n |
microsatellite |
upstream from the MOG transcription start site |
MOG |
1 (0/1/0) |
MTNR1A A/T K334N |
point mutation |
|
MTNR1A |
1 (0/0/1) |
MTNR1A C/G Y170X |
point mutation |
|
MTNR1A |
1 (1/0/0) |
MTNR1A C/T A266V |
point mutation |
|
MTNR1A |
1 (0/0/1) |
MTNR1A G/A G166E |
point mutation |
|
MTNR1A |
1 (0/0/1) |
MTNR1B A/G K243R |
point mutation |
|
MTNR1B |
1 (0/0/1) |
MTNR1B C/T R138C |
point mutation |
|
MTNR1B |
1 (0/0/1) |
MTNR1B G/A G24E |
point mutation |
|
MTNR1B |
1 (0/0/1) |
MTNR1B G/A R231H |
point mutation |
|
MTNR1B |
1 (0/0/1) |
NOS1 Ex1f VNTR |
VNTR |
33 bp downstream of the TATA box |
NOS1 |
1 (1/0/0) |
NR4A2 3'-UTR (CA)n |
microsatellite |
3' UTR |
NR4A2 |
1 (0/1/0) |
NR4A2 upstream deltaC BglI |
point mutation |
254bp upstream from the transcriptional start site, and creates a restriction digest site for BglI |
NR4A2 |
1 (0/1/0) |
SLC6A2 exon5 848C/T |
point mutation |
exon 5 |
SLC6A2 |
1 (0/0/1) |
SLC6A2 exon9 1287G/A Sau96I |
point mutation |
exon 9 |
SLC6A2 |
1 (0/1/0) |
SLC6A2 intron13 1830+66T/C BsiHKAI |
point mutation |
intron 13 |
SLC6A2 |
1 (0/1/0) |
SLC6A2 intron7 C/A BsrDI |
point mutation |
intron 7 |
SLC6A2 |
1 (0/1/0) |
SLC6A3 3'-flanking D5S678 |
microsatellite |
3' flanking |
SLC6A3 |
1 (0/1/0) |
SLC6A3 5'-flanking -3598A>G |
point mutation |
5' flanking sequence/putative promoter |
SLC6A3 |
1 (0/0/1) |
SLC6A3 5'-flanking -3911T>C |
point mutation |
5' flanking sequence/putative promoter |
SLC6A3 |
1 (0/0/1) |
SLC6A3 5'-flanking -4450C>G |
point mutation |
5' flanking sequence/putative promoter |
SLC6A3 |
1 (0/1/0) |
SLC6A3 5'-flanking -4532A>T |
point mutation |
5' flanking sequence/putative promoter |
SLC6A3 |
1 (0/0/1) |
SLC6A3 5'-flanking D5S1981 |
microsatellite |
5' flanking |
SLC6A3 |
1 (1/0/0) |
SLC6A3 exon15 G/C |
point mutation |
exon15 |
SLC6A3 |
1 (0/1/0) |
SLC6A3 exon15 VNTR |
VNTR |
exon15 |
SLC6A3 |
1 (0/1/0) |
SLC6A3 intron1 sid1153 |
point mutation |
intron 1 |
SLC6A3 |
1 (0/1/0) |
SLC6A3 intron3 VNTR |
VNTR |
intron 3 |
SLC6A3 |
1 (0/1/0) |
SLC6A3 intron9 1398-21G->A |
point mutation |
intron 9 |
SLC6A3 |
1 (0/1/0) |
SLC6A3 promoter -67A/T |
point mutation |
core promoter |
SLC6A3 |
1 (1/0/0) |
SLC6A4 D17S1294 |
microsatellite |
|
SLC6A4 |
1 (1/0/0) |
SNAP25 3'-UTR 88268T/C |
point mutation |
3' UTR |
SNAP25 |
1 (0/1/0) |
SNAP25 exon7 80609G/A |
point mutation |
exon 7 |
SNAP25 |
1 (1/0/0) |
SNAP25 hCV2488338 |
point mutation |
|
SNAP25 |
1 (0/1/0) |
SNAP25 hCV27368320 T/C |
point mutation |
|
SNAP25 |
1 (0/1/0) |
SNAP25 intron3 C-2488338-10 |
point mutation |
intron 3 |
SNAP25 |
1 (0/1/0) |
SNAP25 promoter (TG)n |
microsatellite |
promoter |
SNAP25 |
1 (0/1/0) |
SNAP25 promoter -2015A/T |
point mutation |
promoter |
SNAP25 |
1 (1/0/0) |
SNAP25 promoter -900G/T |
point mutation |
promoter |
SNAP25 |
1 (0/1/0) |
TAAR3 A181T |
point mutation |
|
TAAR3 |
1 (0/1/0) |
TDO2 exon7 A(Asn)->C(His) |
point mutation |
exon 7 |
TDO2 |
1 (0/1/0) |
TDO2 intron5 (CCCCT)n |
microsatellite |
3' end of intron 5 |
TDO2 |
1 (0/1/0) |
TDO2 intron6 G->A |
point mutation |
intron 6 |
TDO2 |
1 (0/1/0) |
TDO2 intron6 G->T |
point mutation |
intron 6 |
TDO2 |
1 (1/0/0) |
TPH1 promoter A-6526G |
point mutation |
promoter |
TPH1 |
1 (0/1/0) |