SNP Report
Name | rs555018 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:78586900 - 78586900(+) | ||
Variant Seq | A | ||
Ancestral Allele | A | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.276558 | ||
Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant | ||
Variant Effect | downstream_gene_variant(ENST00000567141); upstream_gene_variant(ENST00000559576); intron_variant(ENST00000299565, ENST00000394802, ENST00000559554) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000299565) | ||
PolyPhen Annotation | possibly_damaging | ||
PolyPhen Variant Effect | possibly_damaging(ENST00000299565) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |