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- Data Summary
SNP Report
Name | rs1055075 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:113239512(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000462711; ENST00000494714; ENST00000575621; ENST00000572987) downstream_gene_variant(ENST00000529221; ENST00000480233; ENST00000483239; ENST00000496311; ENST00000464224; ENST00000314756; ENST00000575184; ENST00000576717; ENST00000574586; ENST00000572649; ENST00000570674) intron_variant(ENST00000393020; ENST00000462711; ENST00000494714; ENST00000575621; ENST00000572987; ENST00000574319) |
||
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.