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

SNP Report

Basic Info
Name rs3892113 dbSNP Ensembl
Location chr18:11876613(Fwd)
Variant Alleles T/G
Ancestral Allele T
Functional Annotation downstream_gene_variant; intron_variant; splice_region_variant.
Consequence to Transcript downstream_gene_variant(ENST00000586926)
intron_variant(ENST00000269162; ENST00000334049; ENST00000423027; ENST00000535121; ENST00000602628)
splice_region_variant(ENST00000269162; ENST00000334049; ENST00000423027; ENST00000535121; ENST00000602628)
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
Laurin N, 2008(b) T/G TDT P-value=0.701, X2=0.148 TDT P-value=0.701, X2=0.148 no significant evidence of association no significant evidence of association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs3892113 (count: 1) View in gBrowse (chr18:11876613..11974749 )
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: 1)