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

SNP Report

Basic Info
Name rs737866 dbSNP Ensembl
Location chr22:19930109(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000361682; ENST00000403184; ENST00000403710; ENST00000407537; ENST00000467943)
nc_transcript_variant(ENST00000467943)
upstream_gene_variant(ENST00000334363; ENST00000400519; ENST00000400521; ENST00000400525; ENST00000474308; ENST00000496729; ENST00000535882; LRG_417t1)
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 T:C T P-value=0.6714, X2=0.18, OR=1.06, 95% CI=0.81-1.4...... P-value=0.6714, X2=0.18, OR=1.06, 95% CI=0.81-1.40 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: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs737866 (count: 6) View in gBrowse (chr22:19921137..19933048 )
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: 6)