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

SNP Report

Basic Info
Name rs829508 dbSNP Ensembl
Location chr3:165502724(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000264381; ENST00000479451; ENST00000482958; ENST00000488954; ENST00000497011; ENST00000540653)
NMD_transcript_variant(ENST00000482958; ENST00000497011)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Jacob CP, 2013 C/T Uncorrected P-value=0.039 Uncorrected P-value=0.039 SNP indicated significant association with ADHD SNP indicated significant association with ADHD Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs829508 (count: 11) View in gBrowse (chr3:165500409..165550036 )
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: 11)