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- Data Summary
SNP Report
Name | rs11611478 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr12:102070089(Fwd) | ||
Variant Alleles | C/T | ||
Ancestral Allele | C | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000548298) intron_variant(ENST00000547405; ENST00000547509; ENST00000550501; ENST00000545503; ENST00000452455; ENST00000550270; ENST00000361685; ENST00000541119; ENST00000361466; ENST00000551300; ENST00000536007; ENST00000392934; ENST00000549608; ENST00000553190; ENST00000441232; ENST00000549145; ENST00000360610) nc_transcript_variant(ENST00000550501; ENST00000549608) |
||
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.