- 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 | rs936470 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:606656(Fwd) | ||
Variant Alleles | G/C | ||
Ancestral Allele | C | ||
Functional Annotation | NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000534320) intron_variant(ENST00000534320; ENST00000413872; ENST00000526724; ENST00000416188; ENST00000533464; ENST00000264555) nc_transcript_variant(ENST00000532550; ENST00000526724) non_coding_exon_variant(ENST00000532550) upstream_gene_variant(ENST00000525848) |
||
No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
Source | LD-proxy |
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.