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

SNP Report

Basic Info
Name rs1800464 dbSNP Ensembl
Location chrX:43571197(Fwd)
Variant Alleles A/C
Ancestral Allele C
Functional Annotation 5_prime_UTR_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant.
Consequence to Transcript 5_prime_UTR_variant(ENST00000542639)
nc_transcript_variant(ENST00000497485)
non_coding_exon_variant(ENST00000497485)
synonymous_variant(ENST00000338702)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Nyman ES, 2007 No available information. No available information. No evidence of association was seen. No evidence of association was seen. Non-significant
Hawi, Z., 2012 A:C A P-value=0.8185, X2=0.053, OR=1.11, 95% CI=0.46-2....... P-value=0.8185, X2=0.053, OR=1.11, 95% CI=0.46-2.66 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: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1800464 (count: 8) View in gBrowse (chrX:43551400..43609617 )
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)