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

SNP Report

Basic Info
Name rs10513003 dbSNP Ensembl
Location chr5:52228442(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; non_coding_exon_variant.
Consequence to Transcript intron_variant(ENST00000282588; ENST00000503559; ENST00000504669; ENST00000505701)
nc_transcript_variant(ENST00000503559; ENST00000504669; ENST00000505701; ENST00000506275)
non_coding_exon_variant(ENST00000506275)
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=0.097 in the catergorical analysis, PICS inat P-valu...... P-value=0.097 in the catergorical analysis, PICS inat P-value=0.013, PICS HI P-value=0.008 in the quantitative analysis More... no significant evidence of association no significant evidence of association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs10513003 (count: 14) View in gBrowse (chr5:52195033..52232558 )
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: 14)