SNP Report
Name | rs58365910 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:78556692 - 78556692(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.220048 | ||
Annotation | downstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000044462) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000560217, ENST00000413382, ENST00000044462, ENST00000559082) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000560217, ENST00000413382, ENST00000044462, ENST00000559082) | ||
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 |