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- Data Summary
SNP Report
Name | rs12628032 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr22:19967980(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000467828; ENST00000492625; ENST00000487793; ENST00000462319) intron_variant(ENST00000406259; ENST00000344269; ENST00000263207; ENST00000401994; ENST00000406522) nc_transcript_variant(ENST00000473551) non_coding_exon_variant(ENST00000473551) upstream_gene_variant(ENST00000480792; ENST00000495096) |
||
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.