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- Data Summary
SNP Report
Name | rs2303940 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr7:150773165(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000460010; ENST00000461979; ENST00000472204; ENST00000540185; ENST00000469355; ENST00000297532; ENST00000482697; ENST00000478477; ENST00000467237; ENST00000469237; ENST00000465272; ENST00000480107; ENST00000496663; ENST00000478883; ENST00000483105; ENST00000493040; ENST00000466855; ENST00000353841; ENST00000460980; ENST00000483953; ENST00000489884; ENST00000494298; ENST00000482806; ENST00000482571; ENST00000459800) nc_transcript_variant(ENST00000485974; ENST00000469467) non_coding_exon_variant(ENST00000485974; ENST00000469467) synonymous_variant(ENST00000413384; ENST00000392826; ENST00000310317; ENST00000461735; ENST00000485713) |
||
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.