SNP Report
| Name | rs9868039 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 3:114127695 - 114127695(+) | ||
| Variant Seq | A | ||
| Ancestral Allele | A | ||
| Ref Seq | G | ||
| Minor Allele Frequence | 0.457867 | ||
| Annotation | downstream_gene_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000460779, ENST00000467632, ENST00000295881, ENST00000383673) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000460779, ENST00000467632, ENST00000295881, ENST00000383673) | ||
| PolyPhen Annotation | possibly_damaging; probably_damaging | ||
| PolyPhen Variant Effect | possibly_damaging(ENST00000295881); probably_damaging(ENST00000460779, ENST00000467632, ENST00000383673) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription | ||
| No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||


