SNP Report
| Name | rs11637635 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 15:78584808 - 78584808(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | A | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.254593 | ||
| Annotation | downstream_gene_variant; intron_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000567141); intron_variant(ENST00000299565, ENST00000559554, ENST00000394802) | ||
| SIFT Annotation | tolerated_-_low_confidence; deleterious_-_low_confidence; tolerated | ||
| SIFT Variant Effect | tolerated_-_low_confidence(ENST00000559554); deleterious_-_low_confidence(ENST00000394802); tolerated(ENST00000559576) | ||
| PolyPhen Annotation | unknown; benign | ||
| PolyPhen Variant Effect | unknown(ENST00000559554); benign(ENST00000394802, ENST00000559576) | ||
| 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 | ||
 
                    


