ADHDgene Database
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  • Large-scale studies
  • Data Summary
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

Other Variant

Search by: Type = otherVariant

Total result: 165

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)

Copyright: Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences Feedback
Last update: Feb 26, 2014