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

SNP Report

Basic Info
Name rs1548364 dbSNP Ensembl
Location chr9:136507742(Fwd)
Variant Alleles A/G
Ancestral Allele G
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000263611; ENST00000393056)
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
Hawi, Z., 2012 G:A G P-value=0.0707, X2=3.27, OR=1.26, 95% CI=0.98-1.6...... P-value=0.0707, X2=3.27, OR=1.26, 95% CI=0.98-1.62 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant
Guan L, 2009 single SNP association analyses: Nominal P-value=0.05, Empir...... single SNP association analyses: Nominal P-value=0.05, Empirical P-value=0.566 for ADHD-I More... non-significant for ADHD, but achieve nominal significance f...... non-significant for ADHD, but achieve nominal significance for ADHD-I More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1548364 (count: 5) View in gBrowse (chr9:136503256..136511385 )
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: 5)