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- Data Summary
SNP Report
Name | rs2677744 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr15:91450441(Fwd) | ||
Variant Alleles | G/A | ||
Ancestral Allele | A | ||
Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | NMD_transcript_variant(ENST00000560451; ENST00000558161) downstream_gene_variant(ENST00000559965; ENST00000559999; ENST00000558853; ENST00000560534; ENST00000558290; ENST00000559132) intron_variant(ENST00000560192; ENST00000558161; ENST00000561046; ENST00000360468; ENST00000560451; ENST00000559717; ENST00000557865) nc_transcript_variant(ENST00000560192; ENST00000561046; ENST00000558640) non_coding_exon_variant(ENST00000558640) upstream_gene_variant(ENST00000560616; ENST00000431652; ENST00000561047; ENST00000558171; ENST00000560505; ENST00000561240; ENST00000559374; ENST00000430376; ENST00000561448) |
||
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.