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

SNP Report

Basic Info
Name rs4998 dbSNP Ensembl
Location chr8:37821486(Fwd)
Variant Alleles C/G
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000345060)
nc_transcript_variant(ENST00000520341)
non_coding_exon_variant(ENST00000520341)
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
Hawi, Z., 2012 G:C C P-value=0.9013, X2=0.02, OR=1.03, 95% CI=0.63-1.6...... P-value=0.9013, X2=0.02, OR=1.03, 95% CI=0.63-1.67 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs4998 (count: 0) View in gBrowse (chr8:37821486..37821486 )