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

SNP Report

Basic Info
Name rs35549391 dbSNP Ensembl
Location chr16:83704419(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation 3_prime_UTR_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Polyphen Annotation: benign(ENST00000268613; ENST00000428848; ENST00000566620)
SIFT Annotation: tolerated(ENST00000268613; ENST00000428848; ENST00000566620)
Consequence to Transcript 3_prime_UTR_variant(ENST00000539548)
missense_variant(ENST00000268613; ENST00000428848; ENST00000566620)
No. of Studies 1 (significant: 0; non-significant: 1; trend: 0)
Source Literature-origin

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result of Statistical Analysis
Mavroconstanti T, 2013 p-value=0.63 p-value=0.63 SNP indicated no significant association with ADHD SNP indicated no significant association with ADHD Non-significant

SNP related genes (count: 1)

Literature-origin genes (count: 1)

Genes from other sources Help (count: 0)

SNPs in LD with rs35549391 (count: 0) View in gBrowse (chr16:83704419..83704419 )