- 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 | rs649266 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr6:16750901(Fwd) | ||
Variant Alleles | T/C | ||
Ancestral Allele | C | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000479680) intron_variant(ENST00000495178; ENST00000473388; ENST00000244769; ENST00000498374; ENST00000467008; ENST00000483954; ENST00000492857; ENST00000296858; ENST00000436367; ENST00000344707; ENST00000450222) nc_transcript_variant(ENST00000473388; ENST00000495178; ENST00000498374; ENST00000467008; ENST00000483954; ENST00000492857) upstream_gene_variant(ENST00000483591) |
||
No. of Studies | 1 (significant: 0; non-significant: 0; trend: 1) | ||
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.