SNP Report
Name | rs9833347 dbSNP Ensembl | ||
---|---|---|---|
Location | 3:42274814 - 42274814(+) | ||
Variant Seq | A | ||
Ancestral Allele | A | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.145367 | ||
Annotation | downstream_gene_variant; upstream_gene_variant | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000334681, ENST00000434608, ENST00000396169) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000334681, ENST00000434608, ENST00000396169) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | Chromatin interactive region | ||
Chromatin State | Enhancers;Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |