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

SNP Report

Basic Info
Name rs2075507 dbSNP Ensembl
Location chr22:19928092(Fwd)
Variant Alleles G/A
Ancestral Allele A
Functional Annotation intron_variant; nc_transcript_variant; NMD_transcript_variant; upstream_gene_variant.
Consequence to Transcript intron_variant(ENST00000334363; ENST00000400519; ENST00000400521; ENST00000400525; ENST00000474308; ENST00000496729; ENST00000535882; LRG_417t1)
nc_transcript_variant(ENST00000474308; ENST00000496729)
upstream_gene_variant(ENST00000361682; ENST00000403184; ENST00000403710; ENST00000407537; ENST00000467943)
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
Michaelovsky E, 2008 A/G P-value=0.045, X2(1)=4.04 P-value=0.045, X2(1)=4.04 showed significant association with ADHD showed significant association with ADHD Significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)

SNPs in LD with rs2075507 (count: 0) View in gBrowse (chr22:19928092..19928092 )