SNP Report
| Name | rs7104301 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 11:34472091 - 34472091(+) | ||
| Variant Seq | G | ||
| Ancestral Allele | A | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.239018 | ||
| Annotation | downstream_gene_variant | ||
| Variant Effect | downstream_gene_variant(ENST00000525707, ENST00000534710, ENST00000241052) | ||
| SIFT Annotation | deleterious; tolerated | ||
| SIFT Variant Effect | deleterious(ENST00000620316, ENST00000429939); tolerated(ENST00000257832, ENST00000312319) | ||
| PolyPhen Annotation | probably_damaging; possibly_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000620316); possibly_damaging(ENST00000257832, ENST00000429939, ENST00000312319) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Strong transcription;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.



