SNP Report
| Name | rs57166361 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 4:33752990 - 33752990(+) | ||
| Variant Seq | C,T | ||
| Ancestral Allele | T | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.26857 | ||
| Annotation | upstream_gene_variant | ||
| SIFT Annotation | deleterious; tolerated | ||
| SIFT Variant Effect | deleterious(ENST00000621961); tolerated(ENST00000511884) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000511884, ENST00000621961) | ||
| rSNP? | No Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Inactive region | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


