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

SNP Report

Basic Info
Name rs2298624 dbSNP Ensembl
Location chr18:47429022(Fwd)
Variant Alleles C/T
Ancestral Allele C
Functional Annotation missense_variant.
Polyphen Annotation: benign(ENST00000285039) | possibly damaging(ENST00000324581; ENST00000592779)
SIFT Annotation: deleterious(ENST00000285039; ENST00000324581; ENST00000592779)
Consequence to Transcript missense_variant(ENST00000285039; ENST00000324581; ENST00000592779)
No. of Studies 0 (significant: 0; non-significant: 0; trend: 0)
Source LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)


SNPs in LD with rs2298624 (count: 0) View in gBrowse (chr18:47429022..47429022 )