SNP Report
| Name | rs2616978 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 8:4620822 - 4620822(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | T | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.492412 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000602557, ENST00000602723, ENST00000400186, ENST00000635120, ENST00000520002) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000520002, ENST00000602723, ENST00000635120, ENST00000602557, ENST00000400186) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000520002, ENST00000602723, ENST00000635120, ENST00000602557, ENST00000400186) | ||
| rSNP? | No Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Inactive region | ||
| No. of Marker's Association Results | 1 (Positive: 0; Negative: 0; Trend: 1) | ||
| 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.



