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

SNP Report

Basic Info
Name rs9973180 dbSNP Ensembl
Location chr18:56954214(Fwd)
Variant Alleles C/T
Ancestral Allele T
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000587244)
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
Neale BM, 2008 T:C Uncorrected TDT P-value=7.05E-05 (OR=0.7489) Uncorrected TDT P-value=7.05E-05 (OR=0.7489) One of top 25 results in uncorrected TDT test One of top 25 results in uncorrected TDT test Non-significant
Lantieri F, 2010 T:C Binomial P-value=0.37, OR=0.96 for whole sample; Binomial P-...... Binomial P-value=0.37, OR=0.96 for whole sample; Binomial P-value=0.69, OR=1.06 for C-subtype More... 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 rs9973180 (count: 28) View in gBrowse (chr18:56945392..57048870 )
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: 28)