SNP Report
| Name | rs77929608 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 2:31584023 - 31584023(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | G | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.0607029 | ||
| Annotation | upstream_gene_variant | ||
| Variant Effect | upstream_gene_variant(ENST00000622030) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000622030) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000622030) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | TF binding region | ||
| Chromatin State | Enhancers;Bivalent Enhancer;Weak transcription | ||
| No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||


