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

SNP Report

Basic Info
Name rs979605 dbSNP Ensembl
Location chrX:43601363(Fwd)
Variant Alleles A/G
Ancestral Allele A
Functional Annotation intron_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000338702; ENST00000542639)
upstream_gene_variant(ENST00000490604)
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 A P-value=0.632, X2=0.229, OR=1.12, 95% CI=0.70-1.7...... P-value=0.632, X2=0.229, OR=1.12, 95% CI=0.70-1.78 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant
Domschke K, 2005 A/G allelic TDT P-value=0.71, X2=0.2, df=1 allelic TDT P-value=0.71, X2=0.2, df=1 did not show any significant distortion in the transmission ...... did not show any significant distortion in the transmission to ADHD cases More... Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs979605 (count: 61) View in gBrowse (chrX:43420059..43612708 )
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: 61)