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- Data Summary
SNP Report
Basic Info
| Name | rs8042868 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr15:43939642(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000433380) downstream_gene_variant(ENST00000419473) intron_variant(ENST00000396923; ENST00000541030) missense_variant(ENST00000321596; ENST00000381761; ENST00000355438; ENST00000396879; ENST00000299989; ENST00000432420; ENST00000433380; ENST00000354127; ENST00000409481) nc_transcript_variant(ENST00000464721; ENST00000469461; ENST00000415968) non_coding_exon_variant(ENST00000464721; ENST00000469461; ENST00000415968) upstream_gene_variant(ENST00000428073) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 4)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 4)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.