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

SNP Report

Basic Info
Name rs362204 dbSNP Ensembl
Location chr22:19956263(Fwd); chr22:19956270(Fwd)
Variant Alleles G/-
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; feature_elongation; NMD_transcript_variant; feature_truncation.
Consequence to Transcript 3_prime_UTR_variant(ENST00000207636; ENST00000361682; ENST00000403710; ENST00000406520; ENST00000407537; ENST00000449653)
downstream_gene_variant(ENST00000263207; ENST00000344269; ENST00000401994; ENST00000403184; ENST00000406259; ENST00000406522; ENST00000412786; ENST00000428707; ENST00000480792; ENST00000493893; ENST00000495096; ENST00000585066)
feature_elongation(ENST00000207636; ENST00000361682; ENST00000403710; ENST00000406520; ENST00000407537; ENST00000449653)
NMD_transcript_variant(ENST00000207636; ENST00000207636; ENST00000361682; ENST00000403710; ENST00000406520; ENST00000407537; ENST00000449653; ENST00000263207; ENST00000344269; ENST00000401994; ENST00000403184; ENST00000406259; ENST00000406522; ENST00000412786; ENST00000428707; ENST00000480792; ENST00000493893; ENST00000495096; ENST00000585066)
feature_truncation(ENST00000207636; ENST00000361682; ENST00000403710; ENST00000406520; ENST00000407537; ENST00000449653; ENST00000207636)
No. of Studies 2 (significant: 1; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 2)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Michaelovsky E, 2008 insC/delC P-value=0.012, X2(1)=6.37 P-value=0.012, X2(1)=6.37 showed significant association with ADHD showed significant association with ADHD Significant
Das M, 2011 C/Del ETDT P-value=0.31, X2(1df)=1.03, RR=1; allelic fr...... ETDT P-value=0.31, X2(1df)=1.03, RR=1; allelic frequencies COCAPHASE P-value=0.84, X2=0.04 for C; ETDT P-value=0.31, X2(1df)=1.03, RR=1.26; allelic frequencies COCAPHASE P-value=0.84, X2=0.04 for Del More... both case-control and family-based analysis failed to show a...... both case-control and family-based analysis failed to show any significant impact More... Non-significant

SNP related genes (count: 3)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 1)


SNPs in LD with rs362204 (count: 0) View in gBrowse (chr22:19956270..19956270 )