SNP Report
Name | rs807060 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:25914964 - 25914964(+) | ||
Variant Seq | T | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.464856 | ||
Annotation | downstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000584862) | ||
SIFT Annotation | deleterious; tolerated | ||
SIFT Variant Effect | deleterious(ENST00000446334, ENST00000426559); tolerated(ENST00000399728, ENST00000455785, ENST00000374291, ENST00000357865) | ||
PolyPhen Annotation | benign; possibly_damaging | ||
PolyPhen Variant Effect | benign(ENST00000399728, ENST00000455785, ENST00000374291, ENST00000357865, ENST00000446334); possibly_damaging(ENST00000426559) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Weak transcription;Enhancers | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |