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 | rs4690194 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr4:760819(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | 3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000362003; ENST00000440452; ENST00000505655; ENST00000521023) NMD_transcript_variant(ENST00000440452) downstream_gene_variant(ENST00000430644; ENST00000470161; ENST00000507446) intron_variant(ENST00000503571) nc_transcript_variant(ENST00000503571) upstream_gene_variant(ENST00000454037) |
||
| 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: 0)
Genes from other sources 
(count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.