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

SNP Report

Basic Info
Name rs11953346 dbSNP Ensembl
Location chr5:94141447(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000312216; ENST00000429576; ENST00000505078; ENST00000508509; ENST00000512425; ENST00000515393; ENST00000573142; ENST00000573439; ENST00000574707; ENST00000575385; ENST00000575480; ENST00000577136)
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
Mick E, 2010 C TDT P-value=1.59E-05 (OR=0.71) TDT P-value=1.59E-05 (OR=0.71) One of the top 20 associations from genome-wide association ...... One of the top 20 associations from genome-wide association results More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs11953346 (count: 10) View in gBrowse (chr5:94046205..94190819 )
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: 10)