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

SNP Report

Basic Info
Name rs11101694 dbSNP Ensembl
Location chr10:135146714(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000252939; ENST00000368554; ENST00000368555; ENST00000368556; ENST00000368558)
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/G allelic ETDT P-value=0.486, X2(1df)=0.486 allelic ETDT P-value=0.486, X2(1df)=0.486 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 rs11101694 (count: 34) View in gBrowse (chr10:135071004..135146714 )
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: 34)