SNP Report
Name | rs25531 dbSNP Ensembl | ||
---|---|---|---|
Location | 17:30237328 - 30237328(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.13758 | ||
Annotation | upstream_gene_variant | ||
Variant Effect | upstream_gene_variant(ENST00000577420, ENST00000394821, ENST00000401766, ENST00000261707) | ||
SIFT Annotation | deleterious_-_low_confidence | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000261714) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000261714) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region | ||
Chromatin State | Bivalent/Poised TSS;Bivalent Enhancer;Enhancers;Weak transcription;Active TSS | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
Source | Literature |