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- Data Summary
SNP Report
Name | rs690466 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr15:43712042(Fwd) | ||
Variant Alleles | C/G | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000411772; ENST00000434561) downstream_gene_variant(ENST00000467474; ENST00000417342) intron_variant(ENST00000263801; ENST00000571145; ENST00000382044; ENST00000450115; ENST00000411772; ENST00000572085; ENST00000434561; ENST00000382039) nc_transcript_variant(ENST00000571145; ENST00000572085) upstream_gene_variant(ENST00000476454) |
||
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.