SNP Report
| Name | rs2267737 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 7:31096996 - 31096996(+) | ||
| Variant Seq | A | ||
| Ancestral Allele | A | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.472444 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000614107, ENST00000409489, ENST00000409363, ENST00000396211, ENST00000304166, ENST00000436116) | ||
| SIFT Annotation | deleterious_-_low_confidence | ||
| SIFT Variant Effect | deleterious_-_low_confidence(ENST00000396211, ENST00000409489, ENST00000614107) | ||
| PolyPhen Annotation | possibly_damaging | ||
| PolyPhen Variant Effect | possibly_damaging(ENST00000396211, ENST00000409489, ENST00000614107) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Enhancers;Strong transcription | ||
| No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
| Source | Literature | ||


