SNP Report
| Name | rs1541518 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 7:31108665 - 31108665(+) | ||
| Variant Seq | T | ||
| Ancestral Allele | T | ||
| Ref Seq | G | ||
| Minor Allele Frequence | 0.399161 | ||
| Annotation | downstream_gene_variant; 3_prime_UTR_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000409363, ENST00000409489, ENST00000396211, ENST00000436116); 3_prime_UTR_variant(ENST00000614107, ENST00000304166) | ||
| SIFT Annotation | deleterious | ||
| SIFT Variant Effect | deleterious(ENST00000436116, ENST00000614107, ENST00000304166, ENST00000409489, ENST00000396211, ENST00000409363) | ||
| PolyPhen Annotation | probably_damaging; possibly_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000409489); possibly_damaging(ENST00000436116, ENST00000614107, ENST00000304166, ENST00000396211, ENST00000409363) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | lncRNA | ||
| Chromatin State | Weak transcription;Strong transcription;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.



