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

SNP Report

Basic Info
Name rs6318 dbSNP Ensembl
Location chrX:113965735(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation missense_variant.
Polyphen Annotation: benign(ENST00000371950; ENST00000276198; ENST00000371951)
SIFT Annotation: deleterious(ENST00000371950) | tolerated(ENST00000276198; ENST00000371951)
Consequence to Transcript missense_variant(ENST00000371950; ENST00000276198; ENST00000371951)
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
Brookes K, 2006 C/G UNPHASED TDT P-value=0.285 UNPHASED TDT P-value=0.285 no significant association was observed no significant association was observed Non-significant
Bobb AJ, 2005 allelic TDT P-value=0.65, OR=1.03 in case-control analysis; ...... allelic TDT P-value=0.65, OR=1.03 in case-control analysis; allelic TDT P-value=0.62, RR=1.29 in family-based analysis More... non-significant association non-significant association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs6318 (count: 187) View in gBrowse (chrX:113815382..114164808 )
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: 187)