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

SNP Report

Basic Info
Name rs11122330 dbSNP Ensembl
Location chr1:231898591(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000295051; ENST00000366632; ENST00000366633; ENST00000366636; ENST00000366637; ENST00000422590; ENST00000439617; ENST00000535944; ENST00000535983; ENST00000537876; ENST00000539444; ENST00000602281; ENST00000602567; ENST00000602634; ENST00000602700; ENST00000602713; ENST00000602822; ENST00000602873; ENST00000602885; ENST00000602956; ENST00000602962)
NMD_transcript_variant(ENST00000295051; ENST00000366632; ENST00000422590; ENST00000535944; ENST00000602567; ENST00000602634; ENST00000602700; ENST00000602713; ENST00000602822; ENST00000602885; ENST00000602956; ENST00000602962)
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
Jacobsen, K. K.,2013 meta-analysis P-value=0.008 ,OR=1.25,95%CI=1.06-1.47 meta-analysis P-value=0.008 ,OR=1.25,95%CI=1.06-1.47 This SNP was significant associated with ADHD in overall met...... This SNP was significant associated with ADHD in overall meta-analysis More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs11122330 (count: 5) View in gBrowse (chr1:231898591..231908769 )
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: 5)