SNP Report
Name | rs8078900 dbSNP Ensembl | ||
---|---|---|---|
Location | 17:30264691 - 30264691(+) | ||
Variant Seq | A | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.252196 | ||
Annotation | downstream_gene_variant; intron_variant; NMD_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000579957, ENST00000577623); intron_variant(ENST00000261714, ENST00000578090); NMD_transcript_variant(ENST00000578090) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000261714) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000261714) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Strong transcription;Active TSS;Genic enhancers;Enhancers;Flanking Active TSS | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |