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

SNP Report

Basic Info
Name rs2032892 dbSNP Ensembl
Location chr5:36677083(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000265113; ENST00000381918)
SIFT Annotation: tolerated(ENST00000265113; ENST00000381918)
Consequence to Transcript intron_variant(ENST00000510740)
missense_variant(ENST00000265113; ENST00000381918)
nc_transcript_variant(ENST00000505376; ENST00000510740)
non_coding_exon_variant(ENST00000505376)
upstream_gene_variant(ENST00000506178)
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
Turic D, 2005(a) C/G(E219D) no P-value no P-value no association no association Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2032892 (count: 3) View in gBrowse (chr5:36669854..36705875 )
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: 3)