SNP Report
| Name | rs6080131 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 20:16125395 - 16125395(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | G | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.441693 | ||
| Annotation | downstream_gene_variant | ||
| SIFT Annotation | deleterious_-_low_confidence; deleterious | ||
| SIFT Variant Effect | deleterious_-_low_confidence(ENST00000407045); deleterious(ENST00000378058, ENST00000402914) | ||
| PolyPhen Annotation | possibly_damaging; probably_damaging | ||
| PolyPhen Variant Effect | possibly_damaging(ENST00000407045); probably_damaging(ENST00000378058, ENST00000402914) | ||
| rSNP? | No Link in rVarBase | ||
| Related Regulatory Elements | N.A. | ||
| Chromatin State | N.A. | ||
| 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.



