SNP Report
| Name | rs6295 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 5:63962738 - 63962738(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | G | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.453275 | ||
| Annotation | upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
| Variant Effect | upstream_gene_variant(ENST00000323865, ENST00000506598); intron_variant(ENST00000502882); non_coding_transcript_variant(ENST00000502882) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000323865) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000323865) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | TF binding region | ||
| Chromatin State | Bivalent/Poised TSS;Active TSS;Flanking Bivalent TSS/Enh;Bivalent Enhancer | ||
| 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.



