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

SNP Report

Basic Info
Name rs17651549 dbSNP Ensembl
Location chr17:44061278(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Polyphen Annotation: possibly damaging(ENST00000262410; ENST00000571987) | probably damaging(ENST00000344290; ENST00000415613)
SIFT Annotation: deleterious(ENST00000262410; ENST00000571987; ENST00000344290; ENST00000415613)
Consequence to Transcript downstream_gene_variant(ENST00000572440)
intron_variant(ENST00000334239; ENST00000340799; ENST00000347967; ENST00000351559; ENST00000420682; ENST00000431008; ENST00000446361; ENST00000535772; ENST00000570299; ENST00000574436; ENST00000576518)
missense_variant(ENST00000262410; ENST00000571987; ENST00000344290; ENST00000415613)
nc_transcript_variant(ENST00000570299; ENST00000576238)
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 rs17651549 (count: 0) View in gBrowse (chr17:44061278..44061278 )