SNP Report
Name | rs10801151 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:192791972 - 192791972(+) | ||
Variant Seq | G | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.295727 | ||
Annotation | upstream_gene_variant | ||
Variant Effect | upstream_gene_variant(ENST00000454090) | ||
SIFT Annotation | deleterious_-_low_confidence; tolerated_-_low_confidence | ||
SIFT Variant Effect | deleterious_-_low_confidence(ENST00000235382); tolerated_-_low_confidence(ENST00000235382) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000235382) | ||
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 |