SNP Report
Name | rs3091244 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:159714875 - 159714875(+) | ||
Variant Seq | A,T | ||
Ancestral Allele | G | ||
Ref Seq | G | ||
Minor Allele Frequence | 0.243011 | ||
Annotation | upstream_gene_variant | ||
Variant Effect | upstream_gene_variant(ENST00000489317, ENST00000437342, ENST00000368111, ENST00000473196, ENST00000368112, ENST00000368110, ENST00000255030) | ||
SIFT Annotation | tolerated | ||
SIFT Variant Effect | tolerated(ENST00000255030) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000255030) | ||
rSNP? | No Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Inactive region | ||
No. of Marker's Association Results | 2 (Positive: 0; Negative: 2; Trend: 0) | ||
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.