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

SNP Report

Basic Info
Name rs17751061 dbSNP Ensembl
Location chr19:19413092(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation 3_prime_UTR_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Polyphen Annotation: probably damaging(ENST00000247001)
SIFT Annotation: deleterious(ENST00000247001)
Consequence to Transcript 3_prime_UTR_variant(ENST00000535070; ENST00000587119; ENST00000588731; ENST00000589144)
downstream_gene_variant(ENST00000334782; ENST00000585444; ENST00000587716; ENST00000588580; ENST00000590439; ENST00000591350; ENST00000606725)
intron_variant(ENST00000585763)
missense_variant(ENST00000247001)
nc_transcript_variant(ENST00000585763; ENST00000586387; ENST00000591007)
NMD_transcript_variant(ENST00000535070; ENST00000587119; ENST00000588731; ENST00000589144)
non_coding_exon_variant(ENST00000586387; ENST00000591007)
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 rs17751061 (count: 0) View in gBrowse (chr19:19413092..19413092 )