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 rs324981 dbSNP Ensembl
Location Chr7:34818113(Fwd)
Variant Alleles A/T
Ancestral Allele T
Functional Annotation NMD_transcript_variant; intron_variant; missense_variant; nc_transcript_variant.
Consequence to Transcript NMD_transcript_variant(ENST00000396095; ENST00000381544)
intron_variant(ENST00000436945; ENST00000539747; ENST00000431669; ENST00000381544; ENST00000442669; ENST00000535640; ENST00000381542)
missense_variant(ENST00000396095; ENST00000359791; ENST00000360581; ENST00000531252; ENST00000381553; ENST00000381539)
nc_transcript_variant(ENST00000436945; ENST00000539747; ENST00000431669; ENST00000442669; ENST00000535640)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Okamura N, 2007 No available information. No available information. No evidence of association was seen. No evidence of association was seen. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs324981 (count: 35) View in gBrowse (chr7:34740832..34866287 )
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: 35)

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