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

SNP Report

Basic Info
Name rs11030101 dbSNP Ensembl
Location chr11:27680744(Fwd)
Variant Alleles A/T
Ancestral Allele A
Functional Annotation 5_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Consequence to Transcript 5_prime_UTR_variant(ENST00000439476; ENST00000525528)
downstream_gene_variant(ENST00000532965)
intron_variant(ENST00000314915; ENST00000356660; ENST00000395978; ENST00000395980; ENST00000395981; ENST00000395983; ENST00000395986; ENST00000418212; ENST00000420794; ENST00000438929; ENST00000525950; ENST00000530786; ENST00000530861; ENST00000532997; ENST00000533131; ENST00000533246; ENST00000584049)
nc_transcript_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000501176; ENST00000502161; ENST00000530313; ENST00000530686; ENST00000584049)
NMD_transcript_variant(ENST00000530786)
non_coding_exon_variant(ENST00000499008; ENST00000499568; ENST00000500662; ENST00000501176; ENST00000502161; ENST00000530313; ENST00000530686)
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
Cho SC, 2010(a) allelic P-value=0.96, X2 (1df)=0, genotypic P-val...... allelic P-value=0.96, X2 (1df)=0, genotypic P-value=0.667, X2 (2df)=0.81 in boys; allelic P-value=0.015, X2 (1df)=5.87, genotypic P-value=0.035 in girls More... the A allele and AA genotype were significantly higher in gi...... the A allele and AA genotype were significantly higher in girls with ADHD than in control girls More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs11030101 (count: 8) View in gBrowse (chr11:27659775..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: 8)