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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
| Name | rs12052787 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr2:234666581(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000446481; ENST00000484784; ENST00000450233) downstream_gene_variant(ENST00000480628; ENST00000506676) intron_variant(ENST00000344644; ENST00000373450; ENST00000373445; ENST00000373426; ENST00000373424; ENST00000354728; ENST00000305139; ENST00000373414; ENST00000373409; ENST00000484784; ENST00000482026; ENST00000450233; ENST00000446481; ENST00000406651) upstream_gene_variant(ENST00000360418; ENST00000305208; ENST00000421868; ENST00000449669; ENST00000450901; ENST00000389816) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.




