- Hot Results
- Quick Search
- 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 | rs2394538 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr10:71033697(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | T | ||
Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | intron_variant(ENST00000450646; ENST00000464803; ENST00000479594; ENST00000480047; ENST00000483077; ENST00000448642; ENST00000476368; ENST00000360289) nc_transcript_variant(ENST00000480047; ENST00000464803; ENST00000479594; ENST00000483077; ENST00000476368) upstream_gene_variant(ENST00000483054; ENST00000488644) |
||
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.