SNP Report
Basic Info
| Name | rs10921541 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 1:194355089 - 194355089(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | T | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.0910543 | ||
| Annotation | downstream_gene_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000435554) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(LRG_507t1, ENST00000367435) | ||
| PolyPhen Annotation | possibly_damaging | ||
| PolyPhen Variant Effect | possibly_damaging(LRG_507t1, ENST00000367435) | ||
| rSNP? | No Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Inactive region | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||
SNP related association results
SNP related genes (count: 0)
SNPs in LD with rs10921541 (count: 0)
SNP related eQTL (count: 1)