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- Data Summary
SNP Report
Basic Info
| Name | rs1043504 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr8:93895897(Fwd) | ||
| Variant Alleles | C/A | ||
| Ancestral Allele | C | ||
| Functional Annotation | 3_prime_UTR_variant; 5_prime_UTR_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | 3_prime_UTR_variant(ENST00000518748; ENST00000521988; ENST00000537541) 5_prime_UTR_variant(ENST00000391681) downstream_gene_variant(ENST00000523580; ENST00000524037; ENST00000519069; ENST00000517540; ENST00000519969; ENST00000518400; ENST00000520686; ENST00000521617; ENST00000522925; ENST00000520430; ENST00000524107; ENST00000517858; ENST00000520384; ENST00000517751; ENST00000378861) intron_variant(ENST00000521203; ENST00000523197) nc_transcript_variant(ENST00000521203; ENST00000523197) upstream_gene_variant(ENST00000523080) |
||
| 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.