SNP Report
Basic Info
| Name | rs3008659 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 1:243860660 - 243860660(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | G | ||
| Ref Seq | G | ||
| Minor Allele Frequence | 0.497604 | ||
| Annotation | upstream_gene_variant | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000263826, ENST00000366540, ENST00000336199, ENST00000552631, ENST00000366539) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000263826, ENST00000366540, ENST00000336199, ENST00000552631, ENST00000366539) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||
SNP related association results
SNP related genes (count: 0)
SNPs in LD with rs3008659 (count: 0)
SNP related eQTL (count: 1)