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

SNP Report

Basic Info
Name rs174548 dbSNP Ensembl
Location chr11:61571348(Fwd)
Variant Alleles C/G
Ancestral Allele G
Functional Annotation 5_prime_UTR_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript 5_prime_UTR_variant(ENST00000460649)
intron_variant(ENST00000350997; ENST00000433932; ENST00000496123; ENST00000536991; ENST00000539999; ENST00000542506; ENST00000574708)
nc_transcript_variant(ENST00000496123)
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
Brookes KJ, 2006(a) C/G allelic P-value=0.9, OR=1.02; TDT P-value=0.191, OR=0.73 (C ...... allelic P-value=0.9, OR=1.02; TDT P-value=0.191, OR=0.73 (C allele), OR=1.37 (G allele); HHRR P-value=0.24, OR=0.94 (C allele), OR=1.21 (G allele) More... was not statistically significant was not statistically significant Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 0)


SNPs in LD with rs174548 (count: 28) View in gBrowse (chr11:61543499..61623140 )
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: 28)