SNP Report
| Name | rs10502692 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 18:38460388 - 38460388(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | C | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.21905 | ||
| Annotation | downstream_gene_variant | ||
| SIFT Annotation | deleterious_-_low_confidence; tolerated_-_low_confidence | ||
| SIFT Variant Effect | deleterious_-_low_confidence(ENST00000601392); tolerated_-_low_confidence(ENST00000420428, ENST00000601019, ENST00000591282, ENST00000588597, ENST00000361795, ENST00000591287, ENST00000334919, ENST00000603232) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000420428, ENST00000601019, ENST00000591282, ENST00000588597, ENST00000361795, ENST00000601392, ENST00000591287, ENST00000334919, ENST00000603232) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Enhancers | ||
| 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.



