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 | rs2270590 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr7:128455916(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | A | ||
| Functional Annotation | intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000378685; ENST00000528772; ENST00000464832; ENST00000464672; ENST00000487361) nc_transcript_variant(ENST00000480137; ENST00000528772; ENST00000471729) non_coding_exon_variant(ENST00000471729; ENST00000480137) synonymous_variant(ENST00000297788; ENST00000494552) |
||
| 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.