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

SNP Report

Basic Info
Name rs16869915 dbSNP Ensembl
Location chr4:20730780(Fwd)
Variant Alleles A/C
Ancestral Allele A
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript 3_prime_UTR_variant(ENST00000382148)
downstream_gene_variant(ENST00000295290; ENST00000359001; ENST00000360916; ENST00000382149; ENST00000382150; ENST00000382152; ENST00000444671; ENST00000447367; ENST00000502374; ENST00000502938; ENST00000503585; ENST00000506552; ENST00000506648; ENST00000506951; ENST00000508952; ENST00000509207; ENST00000513459; ENST00000515786; ENST00000538990)
intron_variant(ENST00000467997; ENST00000471979; ENST00000506702; ENST00000507634)
NMD_transcript_variant(ENST00000467997; ENST00000471979; ENST00000506702)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Weissflog L., 2012 family based test in childhood ADHD sample: p=0.0477 family based test in childhood ADHD sample: p=0.0477 This SNP indicated a nominally significant association with ...... This SNP indicated a nominally significant association with cADHD. More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs16869915 (count: 11) View in gBrowse (chr4:20660406..20732334 )
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: 11)