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 | rs4623937 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:605856(Fwd) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000534320) intron_variant(ENST00000264555; ENST00000534320; ENST00000532550; ENST00000533464; ENST00000413872; ENST00000416188; ENST00000526724) nc_transcript_variant(ENST00000532550; ENST00000526724) upstream_gene_variant(ENST00000525848) |
||
| 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.