Hot Results
- Quick Search
- Large-scale studies
- Genome-wide Association Studies of ADHD
- Genome-wide Linkage Studies of ADHD
- Genome-wide CNV Analyses of ADHD
- Meta-analysis Studies of ADHD
- Data Summary
SNP Report
Basic Info
| Name | rs11149652 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr16:84448005(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | G | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000569207) downstream_gene_variant(ENST00000568160) intron_variant(ENST00000262429; ENST00000416219; ENST00000565631; ENST00000420010; ENST00000569207; ENST00000565546; ENST00000565927) nc_transcript_variant(ENST00000565631; ENST00000420010; ENST00000565546; ENST00000565927) |
||
| 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 
(count: 0)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.