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- Data Summary
SNP Report
Name | rs2229126 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr8:26627672(Fwd) | ||
Variant Alleles | T/A | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000521711; ENST00000519096) downstream_gene_variant(ENST00000518621) intron_variant(ENST00000521711; ENST00000380582; ENST00000519229; ENST00000380586; ENST00000354550; ENST00000519096; ENST00000380587; ENST00000380581) missense_variant(ENST00000380573; ENST00000276393) 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.