SNP Report
| Name | rs9545302 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 13:80027976 - 80027976(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | A | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.476637 | ||
| Annotation | non_coding_transcript_exon_variant; non_coding_transcript_variant | ||
| Variant Effect | non_coding_transcript_exon_variant(ENST00000627044); non_coding_transcript_variant(ENST00000627044) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000487865, ENST00000612570, ENST00000620924, ENST00000218652) | ||
| PolyPhen Annotation | possibly_damaging; probably_damaging | ||
| PolyPhen Variant Effect | possibly_damaging(ENST00000612570, ENST00000620924, ENST00000218652); probably_damaging(ENST00000487865) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription | ||
| No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
| Source | Literature | ||


