SNP Report
| Name | rs1799836 dbSNP Ensembl | ||
|---|---|---|---|
| Location | X:43768752 - 43768752(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | T | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.456689 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000378069) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000378069) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000378069) | ||
| rSNP? | No Link in rVarBase | ||
| Related Regulatory Elements | N.A. | ||
| Chromatin State | N.A. | ||
| No. of Marker's Association Results | 2 (Positive: 1; Negative: 1; Trend: 0) | ||
| Source | Literature | ||


