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- Data Summary
SNP Report
Name | rs2001217 dbSNP Ensembl | ||
---|---|---|---|
Location | Chr15:91498246(Fwd) | ||
Variant Alleles | A/C | ||
Ancestral Allele | A | ||
Functional Annotation | downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
Consequence to Transcript | downstream_gene_variant(ENST00000418476; ENST00000394275; ENST00000471780; ENST00000487875) intron_variant(ENST00000555155; ENST00000555737; ENST00000394258; ENST00000556774) nc_transcript_variant(ENST00000556774; ENST00000555737; ENST00000553321) non_coding_exon_variant(ENST00000553321) upstream_gene_variant(ENST00000554302; ENST00000557266; ENST00000556618; ENST00000556333; ENST00000557750) |
||
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.