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

SNP Report

Basic Info
Name rs7140561 dbSNP Ensembl
Location chr14:39736680(Fwd)
Variant Alleles T/C
Ancestral Allele C
Functional Annotation 5_prime_UTR_variant; intron_variant; missense_variant; nc_transcript_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000280083; ENST00000341502; ENST00000348007; ENST00000396158)
SIFT Annotation: tolerated(ENST00000280083; ENST00000341502; ENST00000348007; ENST00000396158)
Consequence to Transcript 5_prime_UTR_variant(ENST00000556148)
intron_variant(ENST00000341749; ENST00000396165; ENST00000553728; ENST00000554392; ENST00000555716; ENST00000556990; ENST00000557038; ENST00000603904)
missense_variant(ENST00000280083; ENST00000341502; ENST00000348007; ENST00000396158)
upstream_gene_variant(ENST00000553520; ENST00000605298)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 1)

SNPs in LD with rs7140561 (count: 0) View in gBrowse (chr14:39736680..39736680 )