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

SNP Report

Basic Info
Name rs1064608 dbSNP Ensembl
Location chr11:47640429(Fwd)
Variant Alleles G/C
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Polyphen Annotation: probably damaging(ENST00000302503; ENST00000542981)
SIFT Annotation: deleterious(ENST00000302503; ENST00000542981)
Consequence to Transcript downstream_gene_variant(ENST00000530428)
intron_variant(ENST00000539759)
missense_variant(ENST00000302503; ENST00000542981)
nc_transcript_variant(ENST00000525649; ENST00000534074; ENST00000539759)
non_coding_exon_variant(ENST00000525649; ENST00000534074)
upstream_gene_variant(ENST00000411255)
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 rs1064608 (count: 0) View in gBrowse (chr11:47640429..47640429 )