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

SNP Report

Basic Info
Name rs3892170 dbSNP Ensembl
Location chr2:234622412(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant.
Polyphen Annotation: benign(ENST00000373414; ENST00000608381)
SIFT Annotation: tolerated(ENST00000373414; ENST00000608381)
Consequence to Transcript intron_variant(ENST00000305139; ENST00000344644; ENST00000354728; ENST00000373424; ENST00000373426; ENST00000373445; ENST00000373450; ENST00000406651; ENST00000446481; ENST00000478062; ENST00000480628; ENST00000484784; ENST00000609637)
missense_variant(ENST00000373414; ENST00000608381)
nc_transcript_variant(ENST00000478062; ENST00000480628)
NMD_transcript_variant(ENST00000446481; ENST00000484784)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 6)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 5)

SNPs in LD with rs3892170 (count: 0) View in gBrowse (chr2:234622412..234622412 )