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

SNP Report

Basic Info
Name rs10379 dbSNP Ensembl
Location chr1:34330067(Fwd)
Variant Alleles A/C
Ancestral Allele C
Functional Annotation downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000519684; ENST00000522796)
SIFT Annotation: tolerated(ENST00000519684; ENST00000522796)
Consequence to Transcript downstream_gene_variant(ENST00000458277)
intron_variant(ENST00000241312; ENST00000373381)
missense_variant(ENST00000519684; ENST00000522796)
nc_transcript_variant(ENST00000425537)
NMD_transcript_variant(ENST00000241312)
non_coding_exon_variant(ENST00000425537)
upstream_gene_variant(ENST00000425631)
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 rs10379 (count: 0) View in gBrowse (chr1:34330067..34330067 )