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

SNP Report

Basic Info
Name rs8042868 dbSNP Ensembl
Location chr15:43939642(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000321596; ENST00000354127; ENST00000355438; ENST00000381761; ENST00000396879; ENST00000409481; ENST00000432420; ENST00000433380' target='_blank'> ENST00000433380; ENST00000433380' target='_blank'> ENST00000433380)
SIFT Annotation: tolerated(ENST00000321596; ENST00000354127; ENST00000355438; ENST00000381761; ENST00000396879; ENST00000409481; ENST00000432420; ENST00000433380' target='_blank'> ENST00000433380; ENST00000433380' target='_blank'> ENST00000433380)
Consequence to Transcript intron_variant(ENST00000541030)
missense_variant(ENST00000321596; ENST00000354127; ENST00000355438; ENST00000381761; ENST00000396879; ENST00000409481; ENST00000432420; ENST00000433380)
nc_transcript_variant(ENST00000415968; ENST00000464721; ENST00000469461)
NMD_transcript_variant(ENST00000433380)
non_coding_exon_variant(ENST00000415968; ENST00000464721; ENST00000469461)
upstream_gene_variant(ENST00000428073)
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 rs8042868 (count: 0) View in gBrowse (chr15:43939642..43939642 )