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

SNP Report

Basic Info
Name rs200199969 dbSNP Ensembl
Location chr16:83065791(Fwd)
Variant Alleles G/A
Ancestral Allele G
Functional Annotation downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant.
Polyphen Annotation: benign(ENST00000268613; ENST00000428848; ENST00000431540; ENST00000446376; ENST00000565636; ENST00000566620)
SIFT Annotation: tolerated(ENST00000268613; ENST00000428848; ENST00000431540; ENST00000446376; ENST00000565636; ENST00000566620)
Consequence to Transcript downstream_gene_variant(ENST00000562601; ENST00000568770; ENST00000569144)
intron_variant(ENST00000539548)
missense_variant(ENST00000268613; ENST00000428848; ENST00000431540; ENST00000446376; ENST00000565636; ENST00000566620)
nc_transcript_variant(ENST00000566333; ENST00000569454)
NMD_transcript_variant(ENST00000539548)
non_coding_exon_variant(ENST00000566333; ENST00000569454)
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=0.45 p-value=0.45 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 rs200199969 (count: 0) View in gBrowse (chr16:83065791..83065791 )