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

SNP Report

Basic Info
Name rs4663964 dbSNP Ensembl
Location chr2:234650236(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Consequence to Transcript downstream_gene_variant(ENST00000446806; ENST00000449667)
intron_variant(ENST00000305139; ENST00000344644; ENST00000354728; ENST00000373409; ENST00000373414; ENST00000373424; ENST00000373426; ENST00000373445; ENST00000373450; ENST00000406651; ENST00000446481; ENST00000450233; ENST00000480628; ENST00000482026; ENST00000484784; ENST00000608381; ENST00000609637; ENST00000609767)
nc_transcript_variant(ENST00000480628; ENST00000509542)
NMD_transcript_variant(ENST00000446481; ENST00000450233; ENST00000484784)
non_coding_exon_variant(ENST00000509542)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 9)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 8)


SNPs in LD with rs4663964 (count: 0) View in gBrowse (chr2:234650236..234650236 )