SNP Report
Basic Info
| Name | rs8034769 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 15:54445582 - 54445582(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | C | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.0916534 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000260323) | ||
| SIFT Annotation | deleterious_-_low_confidence | ||
| SIFT Variant Effect | deleterious_-_low_confidence(ENST00000260323) | ||
| PolyPhen Annotation | probably_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000260323) | ||
| rSNP? | No Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Inactive region | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||
SNP related association results
SNP related genes (count: 1)
| Approved Symbol | Approved Name | Location | No. of Association Results (Positive/Negative/Trend)  |
|---|---|---|---|
| UNC13C | unc-13 homolog C (C. elegans) | 15q21.3 | 1(0/0/1) |
SNPs in LD with rs8034769 (count: 0)
SNP related eQTL (count: 1)