SNP Report
| Name | rs190526 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 8:130812621 - 130812621(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | A | ||
| Ref Seq | A | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000377928, ENST00000286355) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000377928, ENST00000286355) | ||
| PolyPhen Annotation | probably_damaging; possibly_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000286355); possibly_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 | ||


