SNP Report
                    
                        
                        Basic Info
                        
 
                     
                    
                        
                        
                                | Name | rs211127 
                                    dbSNP
                                    Ensembl | 
                        
                                | Location | 11:17992251 - 17992251(+) | 
                        
                        
                            | Variant Seq | T | 
                        
                        
                        
                            | Ancestral Allele | T | 
                        
                        
                        
                            | Ref Seq | C | 
                        
                        
                        
                            | Minor Allele Frequence | 0.160144 | 
                        
                        
                        
                            | Annotation | downstream_gene_variant; upstream_gene_variant; intron_variant; NMD_transcript_variant; non_coding_transcript_variant | 
                        
                        
                        
                            | Variant Effect | downstream_gene_variant(ENST00000530925, ENST00000533328); upstream_gene_variant(ENST00000533241); intron_variant(ENST00000527494, ENST00000532546, ENST00000532389, ENST00000529728, ENST00000525920, ENST00000530613, ENST00000529151, ENST00000529440, ENST00000528200, ENST00000265965, ENST00000532265, ENST00000525422); NMD_transcript_variant(ENST00000527494, ENST00000532546, ENST00000525422); non_coding_transcript_variant(ENST00000529440) | 
                        
                        
                        
                            | SIFT Annotation | deleterious_-_low_confidence | 
                        
                        
                        
                            | SIFT Variant Effect | deleterious_-_low_confidence(ENST00000530925) | 
                        
                        
                        
                            | PolyPhen Annotation | possibly_damaging | 
                        
                        
                        
                            | PolyPhen Variant Effect | possibly_damaging(ENST00000530925) | 
                        
                        
                            | rSNP? | Yes
                                        
                                        
                                    
                                    Link in rVarBase | 
                        
                            | Related Regulatory Elements | TF binding region;Chromatin interactive region | 
                        
                            | Chromatin State | Weak transcription;Strong transcription;Enhancers | 
                        
                            | No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | 
                        
                            | Source | LD-proxy | 
                    
                     
                    
                    
                        SNP related association results
                        
 
                    
                    
                    
                    
                    
                        
                        SNP related genes (count: 2)
                        
 
                     
                    
                    
                    
                    
                    
                        
                        SNPs in LD with rs211127 (count: 0)
                        
 
                     
                    
                        
                        
                        
                        SNP related eQTL (count: 1)
                        
