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

SNP Report

Basic Info
Name rs7103873 dbSNP Ensembl
Location chr11:27700317(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000499008; ENST00000501176; ENST00000501663; ENST00000530686)
intron_variant(ENST00000314915; ENST00000356660; ENST00000395978; ENST00000395980; ENST00000395981; ENST00000395983; ENST00000395986; ENST00000418212; ENST00000420794; ENST00000438929; ENST00000499568; ENST00000500662; ENST00000502161; ENST00000525950; ENST00000530786; ENST00000530861; ENST00000532997; ENST00000533131; ENST00000533246; ENST00000584049)
nc_transcript_variant(ENST00000499568; ENST00000500662; ENST00000502161; ENST00000584049)
NMD_transcript_variant(ENST00000530786)
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
Tzang RF, 2013 Uncorrected TDT P-value=0.685 Uncorrected TDT P-value=0.685 SNP indicated no significant association with ADHD SNP indicated no significant association with ADHD Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs7103873 (count: 12) View in gBrowse (chr11:27667531..27746991 )
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: 12)