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

SNP Report

Basic Info
Name rs4838721 dbSNP Ensembl
Location chr10:135160950(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000368554; ENST00000423766; ENST00000433452; ENST00000452591; ENST00000458230)
nc_transcript_variant(ENST00000452591)
upstream_gene_variant(ENST00000430526; ENST00000463201)
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
Laurin N, 2005 A/G allelic ETDT P-value=0.03, X2(1df)=4.742 allelic ETDT P-value=0.03, X2(1df)=4.742 TDT statistic was significant TDT statistic was significant Significant

SNP related genes (count: 3)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 3)


SNPs in LD with rs4838721 (count: 15) View in gBrowse (chr10:135071004..135160950 )
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: 15)