SNP Report
| Name | rs1425392 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 4:64526494 - 64526494(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | T | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.249601 | ||
| Annotation | downstream_gene_variant | ||
| SIFT Annotation | tolerated_-_low_confidence; deleterious_-_low_confidence | ||
| SIFT Variant Effect | tolerated_-_low_confidence(ENST00000507440, ENST00000381210); deleterious_-_low_confidence(ENST00000509536) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000509536, ENST00000507440, ENST00000381210) | ||
| rSNP? | No Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Inactive region | ||
| No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
| Source | Literature | ||


