ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

SNP Report

Basic Info
Name rs1801260 dbSNP Ensembl
Location chr4:56301369(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation 3_prime_UTR_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000309964; ENST00000381322; ENST00000513440)
intron_variant(ENST00000506103; ENST00000608091)
nc_transcript_variant(ENST00000511124)
NMD_transcript_variant(ENST00000506103)
non_coding_exon_variant(ENST00000511124)
No. of Studies 2 (significant: 2; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Kissling C, 2008 T/C P-value<0.001 P-value<0.001 a strong, significant association between each of the adult ...... a strong, significant association between each of the adult ADHD assessments and the rs1801260 polymorphism More... Significant
Xu X, 2010 T:C TDT P-value=0.146, X2 (1df)=2.110 for UK samples ...... TDT P-value=0.146, X2 (1df)=2.110 for UK samples allele; TDT P-value=0.010, X2 (1df)=6.701 for Taiwanese samples allele; TDT P-value=0.008, X2 (1df)=7.136 for combined samples allele More... increased transmission of the T allele in the Taiwanese samp...... increased transmission of the T allele in the Taiwanese samples and combined samples; no significant association in the UK sample More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs1801260 (count: 65) View in gBrowse (chr4:56235592..56482750 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 65)