SNP Report
Name | rs182455 dbSNP Ensembl | ||
---|---|---|---|
Location | 1:25908492 - 25908492(+) | ||
Variant Seq | G | ||
Ancestral Allele | G | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.361422 | ||
Annotation | upstream_gene_variant | ||
Variant Effect | upstream_gene_variant(ENST00000465604, ENST00000374291, ENST00000580971, ENST00000446334, ENST00000584862, ENST00000357865, ENST00000455785, ENST00000485226, ENST00000399728, ENST00000426559) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000374291, ENST00000357865, ENST00000455785, ENST00000426559, ENST00000446334, ENST00000399728) | ||
PolyPhen Annotation | benign | ||
PolyPhen Variant Effect | benign(ENST00000374291, ENST00000357865, ENST00000455785, ENST00000426559, ENST00000446334, ENST00000399728) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
Chromatin State | Weak transcription;Enhancers | ||
No. of Marker's Association Results | 5 (Positive: 1; Negative: 4; 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.