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- Data Summary
SNP Report
Basic Info
| Name | rs609230 dbSNP Ensembl | ||
|---|---|---|---|
| Location | Chr12:112146911(Fwd) | ||
| Variant Alleles | C/T | ||
| Ancestral Allele | C | ||
| Functional Annotation | intron_variant; nc_transcript_variant; upstream_gene_variant. | ||
| Consequence to Transcript | intron_variant(ENST00000509936; ENST00000413681; ENST00000455480; ENST00000549590; ENST00000515283; ENST00000392636; ENST00000507135; ENST00000502746; ENST00000313698) nc_transcript_variant(ENST00000502746) upstream_gene_variant(ENST00000552706; ENST00000507683; ENST00000514847) |
||
| 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: 0)
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.