SNP Report
| Name | rs6912833 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 6:35649808 - 35649808(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | T | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.219848 | ||
| Annotation | upstream_gene_variant; intron_variant | ||
| Variant Effect | upstream_gene_variant(ENST00000391277); intron_variant(ENST00000357266, ENST00000536438, ENST00000539068, ENST00000542713) | ||
| SIFT Annotation | deleterious; tolerated | ||
| SIFT Variant Effect | deleterious(ENST00000542713); tolerated(ENST00000539068, ENST00000357266, ENST00000536438) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000539068, ENST00000542713, ENST00000357266, ENST00000536438) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | TF binding region;Chromatin interactive region | ||
| Chromatin State | Weak transcription;Strong transcription;Genic enhancers;Enhancers | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


