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

SNP Report

Basic Info
Name rs957795 dbSNP Ensembl
Location chr21:46758719(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript downstream_gene_variant(ENST00000445242)
nc_transcript_variant(ENST00000416722)
non_coding_exon_variant(ENST00000416722)
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
Neale BM, 2008 A:G Uncorrected TDT P-value=3.86E-05 (OR=0.619) Uncorrected TDT P-value=3.86E-05 (OR=0.619) One of top 25 results in uncorrected TDT test One of top 25 results in uncorrected TDT test Non-significant
Lantieri F, 2010 A:G Binomial P-value=0.98, OR=1.46 for whole sample; Binomial P-...... Binomial P-value=0.98, OR=1.46 for whole sample; Binomial P-value=0.96, OR=1.48 for C-subtype More... no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 1)


SNPs in LD with rs957795 (count: 6) View in gBrowse (chr21:46749718..46759886 )
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)