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

SNP Report

Basic Info
Name rs6505162 dbSNP Ensembl
Location chr17:28444183(Fwd)
Variant Alleles A/C
Ancestral Allele C
Functional Annotation 5_prime_UTR_variant; intron_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Consequence to Transcript 5_prime_UTR_variant(ENST00000585881)
intron_variant(ENST00000247026; ENST00000394826; ENST00000475652; ENST00000479218; ENST00000540900; ENST00000577289; ENST00000582938; ENST00000583301; ENST00000584154; ENST00000584317; ENST00000584423)
nc_transcript_variant(ENST00000362201; ENST00000467446; ENST00000540900; ENST00000577289; ENST00000582938; ENST00000583301; ENST00000586878)
NMD_transcript_variant(ENST00000394826; ENST00000475652; ENST00000584154; ENST00000584317)
non_coding_exon_variant(ENST00000362201; ENST00000467446; ENST00000586878)
upstream_gene_variant(ENST00000580103; ENST00000581048; ENST00000588614; ENST00000589608)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 3)

Literature-origin genes (count: 0)

Genes from other sources Help (count: 3)


SNPs in LD with rs6505162 (count: 0) View in gBrowse (chr17:28444183..28444183 )