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

SNP Report

Basic Info
Name rs3750997 dbSNP Ensembl
Location chr11:71158841(Fwd)
Variant Alleles A/C
Ancestral Allele C
Functional Annotation 5_prime_UTR_variant; intron_variant; upstream_gene_variant.
Consequence to Transcript 5_prime_UTR_variant(ENST00000526780)
intron_variant(ENST00000355527; ENST00000407721; ENST00000525346; ENST00000527316; ENST00000527452; ENST00000529990; ENST00000531364)
upstream_gene_variant(ENST00000529369)
No. of Studies 1 (significant: 0; non-significant: 0; trend: 1)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Neale BM, 2010 (a) A:C P-value=1.62E-05 P-value=1.62E-05 one of top 50 hits from the Genome-Wide Attention-Deficit/Hy...... one of top 50 hits from the Genome-Wide Attention-Deficit/Hyperactivity Disorder (ADHD) meta-analysis More... Trend

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs3750997 (count: 37) View in gBrowse (chr11:71119018..71221248 )
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: 37)