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

SNP Report

Basic Info
Name rs9322993 dbSNP Ensembl
Location chr14:39605542(Fwd)
Variant Alleles T/C
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant.
Consequence to Transcript downstream_gene_variant(ENST00000524781; ENST00000529365; ENST00000531684; ENST00000534684)
intron_variant(ENST00000250379; ENST00000308317; ENST00000396249; ENST00000412033; ENST00000524980; ENST00000525153)
NMD_transcript_variant(ENST00000412033; ENST00000525153)
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
Schimmelmann, B. G.,2013 Nominal two-sided P-value=0.009 (OR=1.51;95%CI=1.10-2.05) Nominal two-sided P-value=0.009 (OR=1.51;95%CI=1.10-2.05) Association signal of nominal p value is below 5%, but it di...... Association signal of nominal p value is below 5%, but it did not survive adjustment for multiple testing. More... Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs9322993 (count: 42) View in gBrowse (chr14:39407138..39788682 )
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: 42)