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

SNP Report

Basic Info
Name rs1048101 dbSNP Ensembl
Location chr8:26628028(Fwd)
Variant Alleles A/G
Ancestral Allele G
Functional Annotation intron_variant; missense_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000276393; ENST00000354550; ENST00000380573; ENST00000380582; ENST00000380586; ENST00000519229)
SIFT Annotation: tolerated(ENST00000276393; ENST00000354550; ENST00000380573; ENST00000380582; ENST00000380586; ENST00000519229)
Consequence to Transcript intron_variant(ENST00000380581; ENST00000380587; ENST00000519096; ENST00000521711)
missense_variant(ENST00000276393; ENST00000354550; ENST00000380573; ENST00000380582; ENST00000380586; ENST00000519229)
nc_transcript_variant(ENST00000518621)
NMD_transcript_variant(ENST00000519096; ENST00000521711)
non_coding_exon_variant(ENST00000518621)
upstream_gene_variant(ENST00000486251)
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
Hawi, Z., 2012 T:C T P-value=0.9475, X2=0, OR=1.01, 95% CI=0.78-1.30 P-value=0.9475, X2=0, OR=1.01, 95% CI=0.78-1.30 The marker did not show significant association with ADHD. The marker did not show significant association with ADHD. Non-significant

SNP related genes (count: 2)

Literature-origin genes (count: 2)

Genes from other sources Help (count: 0)


SNPs in LD with rs1048101 (count: 17) View in gBrowse (chr8:26613408..26669717 )
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.

Literature-origin SNPs (count: 0)

LD-proxies (count: 17)