SNP Report
| Name | rs13278937 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 8:130784244 - 130784244(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | C | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.491613 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000377928, ENST00000286355) | ||
| SIFT Annotation | deleterious; tolerated | ||
| SIFT Variant Effect | deleterious(ENST00000377928); tolerated(ENST00000286355) | ||
| PolyPhen Annotation | benign; probably_damaging | ||
| PolyPhen Variant Effect | benign(ENST00000286355); probably_damaging(ENST00000377928) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


