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

SNP Report

Basic Info
Name rs1000731 dbSNP Ensembl
Location chr1:231963491(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000366632; ENST00000366633; ENST00000366636; ENST00000366637; ENST00000422590; ENST00000427560; ENST00000439617; ENST00000535983; ENST00000537876; ENST00000602713)
nc_transcript_variant(ENST00000427560)
NMD_transcript_variant(ENST00000366632; ENST00000422590; ENST00000602713)
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
Jacobsen, K. K.,2013 chi-square tests P-value=0.58 (OR=1.05;95%CI=0.88-1.25) chi-square tests P-value=0.58 (OR=1.05;95%CI=0.88-1.25) This SNP was not significant associated with ADHD This SNP was not significant associated with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs1000731 (count: 6) View in gBrowse (chr1:231948821..231966862 )
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: 6)