SNP Report
| Name | rs769217 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 11:34461361 - 34461361(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | C | ||
| Ref Seq | C | ||
| Minor Allele Frequence | 0.26278 | ||
| Annotation | downstream_gene_variant; synonymous_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000528104); synonymous_variant(ENST00000241052); non_coding_transcript_exon_variant(ENST00000530343, ENST00000525707); non_coding_transcript_variant(ENST00000530343, ENST00000525707) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000241052) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000241052) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;ZNF genes & repeats;Strong transcription;Enhancers;Genic enhancers | ||
| No. of Marker's Association Results | 1 (Positive: 0; Negative: 1; Trend: 0) | ||
| 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.



