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Large-scale studies
- Genome-wide Association Studies of ADHD
- Genome-wide Linkage Studies of ADHD
- Genome-wide CNV Analyses of ADHD
- Meta-analysis Studies of ADHD
Data Summary
SNP Report
Name | rs2229126 dbSNP Ensembl | ||
---|---|---|---|
Location | chr8:26627672(Fwd) | ||
Variant Alleles | T/A | ||
Ancestral Allele | T | ||
Functional Annotation | downstream_gene_variant; intron_variant; missense_variant; NMD_transcript_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000276393; ENST00000380573) SIFT Annotation: tolerated(ENST00000276393; ENST00000380573) |
||
Consequence to Transcript | downstream_gene_variant(ENST00000518621) intron_variant(ENST00000354550; ENST00000380581; ENST00000380582; ENST00000380586; ENST00000380587; ENST00000519096; ENST00000519229; ENST00000521711) missense_variant(ENST00000276393; ENST00000380573) NMD_transcript_variant(ENST00000519096; ENST00000521711) upstream_gene_variant(ENST00000486251) |
||
No. of Studies | 1 (significant: 1; non-significant: 0; trend: 0) | ||
Source | Literature-origin |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.