SNP Report
| Name | rs3782203 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 12:117282606 - 117282606(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | T | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.153754 | ||
| Annotation | upstream_gene_variant; intron_variant | ||
| Variant Effect | upstream_gene_variant(ENST00000618414); intron_variant(ENST00000344089, ENST00000317775, ENST00000618760, ENST00000338101) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000344089, ENST00000317775, ENST00000338101, ENST00000618760) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000344089, ENST00000317775, ENST00000338101, ENST00000618760) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Strong transcription;Enhancers | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


