SNP Report
| Name | rs514743 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 15:78591885 - 78591885(+) | ||
| Variant Seq | A | ||
| Ancestral Allele | A | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.241214 | ||
| Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000559658, ENST00000326828, ENST00000348639, ENST00000559002); upstream_gene_variant(ENST00000567141); intron_variant(ENST00000394802, ENST00000559576, ENST00000299565, ENST00000559554) | ||
| SIFT Annotation | tolerated_-_low_confidence; deleterious_-_low_confidence; tolerated | ||
| SIFT Variant Effect | tolerated_-_low_confidence(ENST00000348639); deleterious_-_low_confidence(ENST00000348639); tolerated(ENST00000299565) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000348639, ENST00000299565) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | Chromatin interactive region | ||
| Chromatin State | Weak transcription | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


