SNP Report
| Name | rs7754668 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 6:35622315 - 35622315(+) | ||
| Variant Seq | A | ||
| Ancestral Allele | G | ||
| Ref Seq | G | ||
| Minor Allele Frequence | 0.0457268 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000539068, ENST00000542713, ENST00000536438, ENST00000357266) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000536438, ENST00000357266, ENST00000542713, ENST00000539068) | ||
| PolyPhen Annotation | benign; possibly_damaging | ||
| PolyPhen Variant Effect | benign(ENST00000536438, ENST00000357266, ENST00000539068); possibly_damaging(ENST00000542713) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| 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 | ||


