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

SNP Report

Basic Info
Name rs10748185 dbSNP Ensembl
Location chr12:72335855(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000333850; ENST00000546576)
nc_transcript_variant(ENST00000546576)
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
Park, T. W.,2013 G/A allelic chi-square tests P-value=0.889 (OR=1.02; 95%CI=0.73-...... allelic chi-square tests P-value=0.889 (OR=1.02; 95%CI=0.73-1.43; X2=0.14); genotypic chi-square tests P-value=0.238 (OR=0.72; 95%CI=0.42-1.24; X2=1.18). More... No significant difference was reported in this study. No significant difference was reported in this study. Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs10748185 (count: 2) View in gBrowse (chr12:72335855..72338628 )
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: 2)