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.



