ADHDgene Database
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Type:
  • Large-scale studies
  • Data Summary
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

SNP Report

Basic Info
Name rs1349384 dbSNP Ensembl
Location Chr4:21762936(Fwd)
Variant Alleles G/C
Ancestral Allele C
Functional Annotation NMD_transcript_variant; intron_variant; nc_transcript_variant.
Consequence to Transcript NMD_transcript_variant(ENST00000515786)
intron_variant(ENST00000447367; ENST00000382152; ENST00000515786; ENST00000512102)
nc_transcript_variant(ENST00000512102)
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 G case-control test in aADHD sample: P=0.049, OR=1.19, 95%CI=1...... case-control test in aADHD sample: P=0.049, OR=1.19, 95%CI=1.0007-1.4184 More... Nominally significant association findings for KCNIP7 with a...... Nominally significant association findings for KCNIP7 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 rs1349384 (count: 39) View in gBrowse (chr4:21719296..21862428 )
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: 39)

Copyright: Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences Feedback
Last update: Feb 26, 2014