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- Data Summary
SNP Report
Basic Info
| Name | rs1059231 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr6:33288271(Fwd) | ||
| Variant Alleles | A/G | ||
| Ancestral Allele | A | ||
| Functional Annotation | downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant; upstream_gene_variant. | ||
| Consequence to Transcript | downstream_gene_variant(ENST00000446403; ENST00000494082; ENST00000477370; ENST00000446511; ENST00000498030; ENST00000453407) nc_transcript_variant(ENST00000468536; ENST00000477162) non_coding_exon_variant(ENST00000468536; ENST00000477162) synonymous_variant(ENST00000266000; ENST00000414083; ENST00000374542) upstream_gene_variant(ENST00000441117; ENST00000490173; ENST00000418724; ENST00000431845) |
||
| 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.