SNP Report
| Name | rs2134655 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 3:114139354 - 114139354(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | C | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.203275 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000460779, ENST00000295881, ENST00000383673, ENST00000467632) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000295881, ENST00000383673, ENST00000467632, ENST00000460779) | ||
| PolyPhen Annotation | benign; probably_damaging | ||
| PolyPhen Variant Effect | benign(ENST00000295881); probably_damaging(ENST00000383673, ENST00000467632, ENST00000460779) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Enhancers | ||
| No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
| Source | Literature | ||
                    

