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- Data Summary
SNP Report
Basic Info
| Name | rs7932167 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:620599(Fwd) | ||
| Variant Alleles | G/T | ||
| Ancestral Allele | T | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000531177) downstream_gene_variant(ENST00000534311; ENST00000526077; ENST00000529337; ENST00000531088) intron_variant(ENST00000532949; ENST00000349570; ENST00000397542; ENST00000358353; ENST00000531899; ENST00000531177) nc_transcript_variant(ENST00000532949; ENST00000531899) upstream_gene_variant(ENST00000397574; ENST00000348655; ENST00000533182; ENST00000525445; ENST00000532326; ENST00000330243; ENST00000469048; ENST00000533190; ENST00000397562; ENST00000397566; ENST00000532788; ENST00000532096; ENST00000397570) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 2)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.