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

SNP Report

Basic Info
Name rs2161961 dbSNP Ensembl
Location chr18:11774500(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant.
Consequence to Transcript intron_variant(ENST00000269162; ENST00000334049; ENST00000423027; ENST00000535121; ENST00000585642; ENST00000590228; ENST00000590972)
nc_transcript_variant(ENST00000590972)
No. of Studies 1 (significant: 1; non-significant: 0; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Laurin N, 2008(b) A/G TDT P-value=0.011, X2=6.485 for all; TDT P-value=...... TDT P-value=0.011, X2=6.485 for all; TDT P-value=0.005, X2=7.796 for one sib; PDT P-value=0.013; PICS-IV P-value=0.003, PICS-IV P-value=0.008 in the quantitative analysis; A allele P-value=0.005, X2=7.926 for maternal transmission More... demonstrated biased transmission in the categorical analysis...... demonstrated biased transmission in the categorical analysis and significant relationships with dimensional symptoms of inattention and hyperactivity/impulsivity and foudn evidence of strong maternal effect More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2161961 (count: 32) View in gBrowse (chr18:11752943..11828828 )
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: 32)