SNP Report
Basic Info
| Name | rs10993956 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 9:133667290 - 133667290(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | C | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.277356 | ||
| Annotation | upstream_gene_variant; intron_variant | ||
| Variant Effect | upstream_gene_variant(ENST00000469828); intron_variant(ENST00000422262, ENST00000439388, ENST00000371868, ENST00000371872) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000393056) | ||
| PolyPhen Annotation | possibly_damaging | ||
| PolyPhen Variant Effect | possibly_damaging(ENST00000393056) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Strong transcription;Enhancers | ||
| 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)  |
|---|---|---|---|
| SARDH | sarcosine dehydrogenase | 9q33-q34 | Mapped by LD-proxy |
SNPs in LD with rs10993956 (count: 0)
SNP related eQTL (count: 1)