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- Data Summary
SNP Report
Name | rs9905578 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr17:4609640(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | downstream_gene_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000497885) upstream_gene_variant(ENST00000571791; ENST00000570718; ENST00000571347; ENST00000572497; ENST00000575131; ENST00000570823; ENST00000570739; ENST00000574954; ENST00000575101; ENST00000574876; ENST00000436683; ENST00000571764; ENST00000574502; ENST00000269230; ENST00000572457; ENST00000573523; ENST00000466297; ENST00000269260; ENST00000575329; ENST00000575342; ENST00000575877; ENST00000381488; ENST00000346341; ENST00000572293; ENST00000301396; ENST00000412477; ENST00000573886; ENST00000576235; ENST00000570571; ENST00000574888; ENST00000571428) |
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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.