SNP Report
| Name | rs80087508 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 15:78589891 - 78589891(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | A | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.00419329 | ||
| Annotation | downstream_gene_variant; non_coding_transcript_exon_variant; missense_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000348639, ENST00000559658, ENST00000559002); non_coding_transcript_exon_variant(ENST00000567141); missense_variant(ENST00000394802, ENST00000299565); upstream_gene_variant(ENST00000559576); intron_variant(ENST00000559554); non_coding_transcript_variant(ENST00000567141) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000394802, ENST00000299565) | ||
| PolyPhen Annotation | probably_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000394802, ENST00000299565) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Strong transcription | ||
| No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||


