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

SNP Report

Basic Info
Name rs4565946 dbSNP Ensembl
Location chr12:72336769(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000333850; ENST00000546576)
nc_transcript_variant(ENST00000546576)
No. of Studies 2 (significant: 0; non-significant: 2; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Walitza S, 2005 C/T allelic PDT P-value (two-sided)=0.3517 allelic PDT P-value (two-sided)=0.3517 no transmission distortion was observed no transmission distortion was observed Non-significant
Johansson S, 2010 logistic regression P-value=0.79, OR=1.02 logistic regression P-value=0.79, OR=1.02 no significant association no significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs4565946 (count: 1) View in gBrowse (chr12:72335988..72336769 )
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: 1)