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

SNP Report

Basic Info
Name rs8050136 dbSNP Ensembl
Location chr16:53816275(Fwd)
Variant Alleles C/A
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000394647; ENST00000464071; ENST00000471389; ENST00000570395)
nc_transcript_variant(ENST00000570395)
NMD_transcript_variant(ENST00000464071)
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
Choudhry, Z.,2013 A/C FTO SNP rs8050136 was marginally associated with ADHD diagno...... FTO SNP rs8050136 was marginally associated with ADHD diagnosis (P < 0.05) More... This SNP was significant associated with ADHD This SNP was significant associated with ADHD Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs8050136 (count: 37) View in gBrowse (chr16:53799507..53845487 )
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: 37)