SNP Report
| Name | rs7804958 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 7:31078571 - 31078571(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | G | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.0623003 | ||
| Annotation | downstream_gene_variant; intron_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000431811); intron_variant(ENST00000614107, ENST00000409489, ENST00000396211, ENST00000409363, ENST00000304166) | ||
| SIFT Annotation | tolerated | ||
| SIFT Variant Effect | tolerated(ENST00000431811, ENST00000614107, ENST00000396211, ENST00000409489, ENST00000304166, ENST00000409363) | ||
| PolyPhen Annotation | benign; probably_damaging; possibly_damaging | ||
| PolyPhen Variant Effect | benign(ENST00000431811, ENST00000409489, ENST00000304166); probably_damaging(ENST00000409363); possibly_damaging(ENST00000614107, ENST00000396211) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;ZNF genes & repeats;Strong transcription;Genic enhancers;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.



