SNP Report
| Name | rs1049862 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 10:60029514 - 60029514(+) | ||
| Variant Seq | A | ||
| Ancestral Allele | G | ||
| Ref Seq | G | ||
| Minor Allele Frequence | 0.280152 | ||
| Annotation | downstream_gene_variant; 3_prime_UTR_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000489505, ENST00000480699, ENST00000503366, ENST00000618374, ENST00000355288, ENST00000502769, ENST00000612776); 3_prime_UTR_variant(ENST00000373827, ENST00000373820, ENST00000280772) | ||
| SIFT Annotation | tolerated_-_low_confidence | ||
| SIFT Variant Effect | tolerated_-_low_confidence(ENST00000263102) | ||
| PolyPhen Annotation | benign | ||
| PolyPhen Variant Effect | benign(ENST00000263102) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Enhancers;Flanking Active TSS | ||
| 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.



