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

SNP Report

Basic Info
Name rs430665 dbSNP Ensembl
Location chr5:112228667(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Polyphen Annotation: unknown(ENST00000391338)
SIFT Annotation: deleterious(ENST00000391338)
Consequence to Transcript downstream_gene_variant(ENST00000503445; ENST00000506997; ENST00000509024)
intron_variant(ENST00000261482; ENST00000379638; ENST00000474542; ENST00000497856; ENST00000504247; ENST00000511865; ENST00000513339; ENST00000545426)
missense_variant(ENST00000391338)
nc_transcript_variant(ENST00000474542; ENST00000497856; ENST00000512790)
NMD_transcript_variant(ENST00000511865)
non_coding_exon_variant(ENST00000512790)
upstream_gene_variant(ENST00000602872)
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 rs430665 (count: 0) View in gBrowse (chr5:112228667..112228667 )