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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 | rs2032892 dbSNP Ensembl | ||
---|---|---|---|
Location | chr5:36677083(Fwd) | ||
Variant Alleles | G/C | ||
Ancestral Allele | G | ||
Functional Annotation | intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant.
Polyphen Annotation: benign(ENST00000265113; ENST00000381918) SIFT Annotation: tolerated(ENST00000265113; ENST00000381918) |
||
Consequence to Transcript | intron_variant(ENST00000510740) missense_variant(ENST00000265113; ENST00000381918) nc_transcript_variant(ENST00000505376; ENST00000510740) non_coding_exon_variant(ENST00000505376) upstream_gene_variant(ENST00000506178) |
||
No. of Studies | 1 (significant: 0; non-significant: 1; 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.