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- Data Summary
SNP Report
Name | rs3736025 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr8:23112662(Fwd) | ||
Variant Alleles | C/T | ||
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(ENST00000517325; ENST00000519414; ENST00000519503) intron_variant(ENST00000517325; ENST00000519414; ENST00000397677; ENST00000313219; ENST00000519503; ENST00000519529; ENST00000519984) nc_transcript_variant(ENST00000523091; ENST00000519529) non_coding_exon_variant(ENST00000523091) upstream_gene_variant(ENST00000520102; ENST00000521656) |
||
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.