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- Data Summary
SNP Report
Basic Info
| Name | rs2242511 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr11:47441664(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | downstream_gene_variant; intron_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000528362; ENST00000524886; ENST00000526993; ENST00000531653; ENST00000524928; ENST00000362021; ENST00000527829; ENST00000354884; ENST00000524447; ENST00000527906; ENST00000533076; ENST00000530887; ENST00000530651; ENST00000531051) intron_variant(ENST00000530912; ENST00000298852) |
||
| 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: 1)
Genes from other sources 
(count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2>=0.8.