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

SNP Report

Basic Info
Name rs11191580 dbSNP Ensembl
Location chr10:104906211(Fwd)
Variant Alleles T/C
Ancestral Allele T
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000343289; ENST00000369857; ENST00000404739; ENST00000423468; ENST00000452156; ENST00000461461; ENST00000470299)
nc_transcript_variant(ENST00000369857)
NMD_transcript_variant(ENST00000452156; ENST00000461461)
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
PGC, 2013 T/C P-value=1¡¤11E-08 for five disorders combined P-value=1¡¤11E-08 for five disorders combined Significant association was observed in cross-disorder analy...... Significant association was observed in cross-disorder analysis. More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs11191580 (count: 35) View in gBrowse (chr10:104707016..104939215 )
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: 35)