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- Data Summary
SNP Report
Name | rs17722979 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr4:56346411(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | G | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000435527) downstream_gene_variant(ENST00000509151) intron_variant(ENST00000309964; ENST00000513440; ENST00000381322; ENST00000506923; ENST00000435527; ENST00000506747) nc_transcript_variant(ENST00000506923; ENST00000506747) upstream_gene_variant(ENST00000508049) |
||
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.