SNP Report
| Name | rs2214837 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 7:30634164 - 30634164(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | A | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.399561 | ||
| Annotation | downstream_gene_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000496643, ENST00000485784, ENST00000389266, ENST00000444666, ENST00000465748, LRG_243t1) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000389266, ENST00000444666, LRG_243t1) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000389266, ENST00000444666, LRG_243t1) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | Chromatin interactive region | ||
| Chromatin State | Strong transcription;Weak transcription;Genic enhancers;Enhancers | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


