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

SNP Report

Basic Info
Name rs12646862 dbSNP Ensembl
Location chr4:21922119(Fwd)
Variant Alleles A/C
Ancestral Allele A
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000382152; ENST00000447367; ENST00000515786)
NMD_transcript_variant(ENST00000515786)
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
Weissflog L., 2012 C case-control test in aADHD sample: P=0.0147, OR=1.27, 95%CI=...... case-control test in aADHD sample: P=0.0147, OR=1.27, 95%CI=1.0481-1.5371 More... Nominally significant association findings for KCNIP9 with a...... Nominally significant association findings for KCNIP9 with adult ADHD. More... Significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs12646862 (count: 24) View in gBrowse (chr4:21911866..21973739 )
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: 24)