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

SNP Report

Basic Info
Name rs6271 dbSNP Ensembl
Location chr9:136522274(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation missense_variant; nc_transcript_variant; non_coding_exon_variant.
Polyphen Annotation: possibly damaging(ENST00000393056)
SIFT Annotation: tolerated(ENST00000393056)
Consequence to Transcript missense_variant(ENST00000393056)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Hawi, Z., 2012 C:T C P-value=0.1892, X2=1.72, OR=1.42, 95% CI=0.85-2.3...... P-value=0.1892, X2=1.72, OR=1.42, 95% CI=0.85-2.37 More... The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs6271 (count: 1) View in gBrowse (chr9:136477511..136522274 )
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: 1)