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- Data Summary
SNP Report
Basic Info
| Name | rs12466997 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr2:234656517(Fwd) | ||
| Variant Alleles | T/C | ||
| Ancestral Allele | T | ||
| Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000484784; ENST00000446481; ENST00000450233) intron_variant(ENST00000373424; ENST00000344644; ENST00000373426; ENST00000373445; ENST00000354728; ENST00000480628; ENST00000373450; ENST00000482026; ENST00000484784; ENST00000373409; ENST00000446481; ENST00000406651; ENST00000373414; ENST00000305139; ENST00000450233) nc_transcript_variant(ENST00000480628; ENST00000454886) non_coding_exon_variant(ENST00000454886) upstream_gene_variant(ENST00000506676; ENST00000446806; ENST00000449667) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 10)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 9)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.