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

SNP Report

Basic Info
Name rs1001220 dbSNP Ensembl
Location chr7:73110603(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(ENST00000222812; ENST00000395154; ENST00000395155; ENST00000395156; ENST00000428163; ENST00000432522; ENST00000441822; ENST00000478670; ENST00000480126; ENST00000484736; ENST00000487006; ENST00000491427; ENST00000491645; ENST00000496153; ENST00000496216; ENST00000497980)
intron_variant(ENST00000265758; ENST00000421744; ENST00000423166; ENST00000423497; ENST00000430270; ENST00000430446; ENST00000436944; ENST00000442099; ENST00000453316; ENST00000463307)
nc_transcript_variant(ENST00000463307; ENST00000471215)
NMD_transcript_variant(ENST00000421744; ENST00000430270; ENST00000430446; ENST00000436944)
non_coding_exon_variant(ENST00000471215)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 2)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 1)


SNPs in LD with rs1001220 (count: 0) View in gBrowse (chr7:73110603..73110603 )