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- Data Summary
SNP Report
Basic Info
| Name | rs1266489 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr15:91458485(Fwd) | ||
| Variant Alleles | G/A | ||
| Ancestral Allele | A | ||
| Functional Annotation | NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant. | ||
| Consequence to Transcript | NMD_transcript_variant(ENST00000560451; ENST00000561448; ENST00000558161) downstream_gene_variant(ENST00000561047; ENST00000560522; ENST00000560505; ENST00000561240; ENST00000560616; ENST00000559374; ENST00000560192; ENST00000558171) intron_variant(ENST00000431652; ENST00000560451; ENST00000561448; ENST00000557990; ENST00000557865; ENST00000430376; ENST00000360468; ENST00000560147; ENST00000558161; ENST00000559717) upstream_gene_variant(ENST00000560880; ENST00000559704; ENST00000560926; ENST00000558538; ENST00000558374; ENST00000559341; ENST00000559558) |
||
| No. of Studies | 0 (significant: 0; non-significant: 0; trend: 0) | ||
| Source | LD-proxy | ||
SNP related studies (count: 0)
SNP related genes (count: 1)
Literature-origin genes (count: 1)
Genes from other sources 
(count: 0)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.