SNP Report
Name | rs1509856 dbSNP Ensembl | ||
---|---|---|---|
Location | 8:130779582 - 130779582(+) | ||
Variant Seq | C | ||
Ancestral Allele | T | ||
Ref Seq | T | ||
Minor Allele Frequence | 0.495208 | ||
Annotation | downstream_gene_variant | ||
Variant Effect | downstream_gene_variant(ENST00000377928, ENST00000286355) | ||
SIFT Annotation | tolerated_-_low_confidence; deleterious_-_low_confidence | ||
SIFT Variant Effect | tolerated_-_low_confidence(ENST00000286355); deleterious_-_low_confidence(ENST00000377928, ENST00000286355) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000377928, ENST00000286355) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Enhancers;Weak transcription | ||
No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
Source | LD-proxy |