SNP Report
Basic Info
| Name | rs4756146 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 11:34442192 - 34442192(+) | ||
| Variant Seq | C | ||
| Ancestral Allele | T | ||
| Ref Seq | T | ||
| Minor Allele Frequence | 0.134385 | ||
| Annotation | intron_variant | ||
| Variant Effect | intron_variant(ENST00000241052) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000241052) | ||
| PolyPhen Annotation | probably_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000241052) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | Chromatin interactive region | ||
| Chromatin State | Weak transcription;Active TSS;Strong transcription;Enhancers;ZNF genes & repeats;Genic enhancers;Flanking Active TSS | ||
| 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)  |
|---|---|---|---|
| CAT | catalase | 11p13 | 1(1/0/0) |
SNPs in LD with rs4756146 (count: 0)
SNP related eQTL (count: 1)