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

SNP Report

Basic Info
Name rs10491412 dbSNP Ensembl
Location chr5:50671121(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript downstream_gene_variant(ENST00000558403; ENST00000559112)
nc_transcript_variant(ENST00000601500)
non_coding_exon_variant(ENST00000601500)
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
Laurin N, 2008(a) C/T P-value=0.438 in the catergorical analysis, P-value>0.05 in ...... P-value=0.438 in the catergorical analysis, P-value>0.05 in the quantitative analysis More... no significant evidence of association no significant evidence of association Non-significant

SNP related genes (count: 0)

SNPs in LD with rs10491412 (count: 1) View in gBrowse (chr5:50492629..50671121 )
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: 1)