SNP Report
Name | rs9725031 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:232308709 - 232308709(+) | ||
Variant Seq | T | ||
Ancestral Allele | C | ||
Ref Seq | C | ||
Minor Allele Frequence | 0.122005 | ||
Annotation | downstream_gene_variant; upstream_gene_variant | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000439617, ENST00000366637, ENST00000620189) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000439617, ENST00000366637, ENST00000620189) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Enhancers | ||
No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
Source | Literature |
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.