SNP Report
| Name | rs7604404 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 2:172443590 - 172443590(+) | ||
| Variant Seq | A | ||
| Ancestral Allele | A | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.359824 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000442250, ENST00000458358, ENST00000409080, ENST00000409532, ENST00000412899, ENST00000264107) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000409080, ENST00000264107, ENST00000458358, ENST00000442250) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000409080, ENST00000264107, ENST00000458358, ENST00000442250) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | Chromatin interactive region;lncRNA | ||
| Chromatin State | Enhancers;Weak transcription;Genic enhancers | ||
| No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
| Source | Literature | ||
The LD data used here is based on 1000 Genome Phase I. LD SNP pairs were selected with a threshold r2<=0.8.



