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- Data Summary
SNP Report
Name | rs12496777 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr3:114066149(Fwd) | ||
Variant Alleles | A/G | ||
Ancestral Allele | A | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000470311) intron_variant(ENST00000462705; ENST00000357258; ENST00000481632; ENST00000471418; ENST00000474710; ENST00000479879; ENST00000464560; ENST00000393785) nc_transcript_variant(ENST00000479879) upstream_gene_variant(ENST00000475939; ENST00000496219; ENST00000467304) |
||
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.