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

SNP Report

Basic Info
Name rs607138 dbSNP Ensembl
Location chr6:16749567(Fwd)
Variant Alleles A/G
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000479680)
intron_variant(ENST00000244769; ENST00000436367; ENST00000467008; ENST00000473388; ENST00000483591; ENST00000483954; ENST00000492857; ENST00000495178; ENST00000498374)
nc_transcript_variant(ENST00000467008; ENST00000473388; ENST00000483591; ENST00000483954; ENST00000492857; ENST00000495178; ENST00000498374)
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:G P-value=1.69E-05 P-value=1.69E-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 rs607138 (count: 10) View in gBrowse (chr6:16731227..16758112 )
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: 10)