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- Data Summary
SNP Report
Name | rs7924316 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr11:2173447(Fwd) | ||
Variant Alleles | T/G | ||
Ancestral Allele | T | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000356578) downstream_gene_variant(ENST00000381363; ENST00000445504; ENST00000381361) intron_variant(ENST00000481781; ENST00000356578; ENST00000397270; ENST00000381319; ENST00000476874) nc_transcript_variant(ENST00000481781; ENST00000476874) upstream_gene_variant(ENST00000300632; ENST00000337883) |
||
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.