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

SNP Report

Basic Info
Name rs2298122 dbSNP Ensembl
Location chr10:135141572(Fwd)
Variant Alleles G/T
Ancestral Allele G
Functional Annotation intron_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000252939; ENST00000368554; ENST00000368555; ENST00000368556; ENST00000368558)
upstream_gene_variant(ENST00000467433; ENST00000467611; ENST00000605518)
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, 2005 A/C allelic ETDT P-value=0.124, X2(1df)=2.368 allelic ETDT P-value=0.124, X2(1df)=2.368 TDT statistic was not significant TDT statistic was not significant Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs2298122 (count: 16) View in gBrowse (chr10:135071004..135141572 )
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: 16)