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 | rs10134508 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr14:59351820(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | intron_variant; nc_transcript_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000555378; ENST00000553762; ENST00000556815) nc_transcript_variant(ENST00000553762; ENST00000556815; ENST00000555378) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 0)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.
