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

SNP Report

Basic Info
Name rs9332377 dbSNP Ensembl
Location chr22:19955692(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; NMD_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000263207; ENST00000344269; ENST00000401994; ENST00000403184; ENST00000406259; ENST00000406522; ENST00000428707; ENST00000480792; ENST00000493893; ENST00000495096; ENST00000585066)
intron_variant(ENST00000207636; ENST00000361682; ENST00000403710; ENST00000406520; ENST00000407537; ENST00000412786; ENST00000449653)
NMD_transcript_variant(ENST00000207636)
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
Hawi, Z., 2012 C:T C P-value=0.7079, X2=0.14, OR=1.07, 95% CI=0.65-1.4...... P-value=0.7079, X2=0.14, OR=1.07, 95% CI=0.65-1.43 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 3)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 1)


SNPs in LD with rs9332377 (count: 3) View in gBrowse (chr22:19955692..19991067 )
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: 3)