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- Data Summary
SNP Report
Basic Info
| Name | rs2278860 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr15:43659046(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000566849) downstream_gene_variant(ENST00000563508; ENST00000561661) intron_variant(ENST00000562072; ENST00000568898; ENST00000396976; ENST00000566849; ENST00000396972; ENST00000570181) upstream_gene_variant(ENST00000564079; ENST00000563517; ENST00000570081; ENST00000260383) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 2)
Literature-origin genes (count: 0)
Genes from other sources 
(count: 2)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.