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

SNP Report

Basic Info
Name rs3760201 dbSNP Ensembl
Location chr17:21193618(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000316920; ENST00000342679; ENST00000361818; ENST00000395491; ENST00000479129; ENST00000483928; ENST00000496046; ENST00000526076; ENST00000529517; ENST00000534743; ENST00000583508)
nc_transcript_variant(ENST00000534743; ENST00000583508)
NMD_transcript_variant(ENST00000395491; ENST00000479129; ENST00000483928; ENST00000496046)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hinney, A., 2011 T GWAS P-value=2.05E-05, OR=1.44, Replication FBAT P-value=0.2...... GWAS P-value=2.05E-05, OR=1.44, Replication FBAT P-value=0.2466, Combination P-value=1.84E-05 More... This GWAS in a small group of clinically ascertained young G...... This GWAS in a small group of clinically ascertained young German patients with ADHD and population-based controls did not reveal genome-wide significant findings. Replication attempts in further German and international samples did also not lead to a P-value(s) below 5E-08. More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs3760201 (count: 8) View in gBrowse (chr17:21172289..21215204 )
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: 8)